AuroMedics Pharma LLC
Código de etiquetadora NDC: 55150
¿Qué es una etiquetadora?
La empresa cuyo nombre aparece en el envase y en el directorio de códigos nacionales de medicamentos (NDC) de la FDA. Puede fabricar el medicamento o vender uno fabricado por otra empresa. La primera parte de cada código NDC identifica a la etiquetadora.
Solo datos oficiales de la FDA
Los productos, aprobaciones y retiros vienen de la FDA (directorio NDC, Drugs@FDA, informes de retiros). Los retiros se vinculan a esta empresa por el código NDC del producto retirado.
Si tiene preguntas sobre su medicamento, hable con su médico o farmacéutico. En una emergencia, llame al 911.
Medicamentos con receta
- GlycopyrrolateGlyrx-Pf, Glycate, Cuvposa · 4 productos
- Amiodarone hydrochloridePacerone, Nexterone · 3 productos
- AcyclovirZovirax, Avaclyr · 2 productos
- Atracurium besylate2 productos
- CyanocobalaminNascobal · 1 producto
- Zoledronic acidReclast · 1 producto
- Sodium nitroprussideNipride Rtu · 1 producto
Solicitudes de la FDA de estos productos
- ANDA: Solicitud abreviada (ANDA): así se aprueba una versión genérica.
| Aprobada | Solicitud | Medicamento | Patrocinador |
|---|---|---|---|
| 10 de diciembre de 2020 | ANDA211934 | Sodium nitroprusside SODIUM NITROPRUSSIDE | Eugia Pharma |
| 8 de diciembre de 2020 | ANDA213874 | Cyanocobalamin CYANOCOBALAMIN | Eugia Pharma |
| 28 de noviembre de 2018 | ANDA210244 | Glycopyrrolate GLYCOPYRROLATE | Eugia Pharma |
| 25 de octubre de 2017 | ANDA204550 | Amiodarone hydrochloride AMIODARONE HYDROCHLORIDE | Eugia Pharma |
| 26 de septiembre de 2016 | ANDA207751 | Zoledronic acid ZOLEDRONIC ACID | Eugia Pharma |
| 8 de abril de 2015 | ANDA206010 | Atracurium besylate ATRACURIUM BESYLATE PRESERVATIVE FREE | Eugia Pharma |
| 8 de abril de 2015 | ANDA206011 | Atracurium besylate ATRACURIUM BESYLATE | Eugia Pharma |
| 11 de octubre de 2013 | ANDA203701 | Acyclovir ACYCLOVIR SODIUM | Eugia Pharma |
El patrocinador es la empresa titular de la solicitud ante la FDA; puede ser distinta de la etiquetadora.
Cronología de retiros
2026
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15 de julio de 2026 · Clase III · En curso · D-0713-2026 · Lidocaine, Triamcinolone acetonide
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 76420-760-01.
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18 de mayo de 2026 · Clase III · En curso · D-0552-2026 · Lidocaine, Triamcinolone acetonide
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02
2025
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29 de mayo de 2025 · Clase II · En curso · D-0472-2025 · Gentamicin sulfate
Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.
Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ, 08520 Vial- NDC 55150-401-01, Carton NDC 55150-401-25
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21 de abril de 2025 · Clase II · En curso · D-0390-2025 · Tirofiban
Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL), 250 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-430-01
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21 de abril de 2025 · Clase II · En curso · D-0389-2025 · Tirofiban
Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL), 100 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-429-01
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10 de abril de 2025 · Clase II · En curso · D-0363-2025 · Testosterone cypionate
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial, Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, India, NDC 55150-277-01
2024
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27 de diciembre de 2024 · Clase II · En curso · D-0186-2025 · Progesterone
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
Progesterone Injection USP, 500mg per 10 mL (50mg/mL), 10 mL Multiple Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor NJ 08520 NDC # 55150-306-10
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18 de diciembre de 2024 · Clase II · En curso · D-0185-2025 · Medroxyprogesterone acetate
CGMP Deviations
medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL, Rx only, 1 mL Single-Dose Vial, Mfd in India for: Eugia US LLC, NJ 08520 NDC 55150-329-01 Shipper label: medroxyPROGESTERone Acetate Injectable Suspen
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26 de julio de 2024 · Clase II · En curso · D-0624-2024 · Progesterone
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Progesterone Injection, USP, 500 mg per 10 mL (50mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E Windsor, NJ 08520, NDC 55150-306-10.
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23 de mayo de 2024 · Clase II · En curso · D-0555-2024 · Dexamethasone
Failed Impurities/Degradation Specifications: impurity sulfonic acid adduct of dexamethasone phosphate results were above spec.
Dexamethasone Sodium Phosphate injection USP, 120mg per 30mL (4mg/mL), 30 mL Multiple-Dose Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520, Made in India, NDC 55150
Mostrar los 40 retiros anteriores
2024
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22 de mayo de 2024 · Clase III · En curso · D-0556-2024 · Eptifibatide
Failed Impurities/Degradation Specifications: failed related substance identified as Eptifibatide dimer.
Eptifibatide injection 20mg/10mL (2mg/mL), 10mL Single-Dose Vial, Rx only, Mfd. In India for: AuroMedics Pharma, LLC, E. Windsor, NJ 08520, NDC 55150-219-10
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22 de febrero de 2024 · Clase II · Cerrado por la FDA · D-0385-2024 · Tobramycin
Failed Stability Specification: Water determination was found not complying with specification.
Tobramycin for Injection, USP, 1.2 grams per Pharmacy Bulk Package, Rx Only, For Intravenous Use, PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, Carton NDC 55150-470
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20 de febrero de 2024 · Clase II · En curso · D-0390-2024 · Nicardipine
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 NDC 55150-183-10
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20 de febrero de 2024 · Clase II · En curso · D-0391-2024 · Nicardipine
Failed Impurities/Degradation Specifications: Out of specification for organic impurities
Nicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) 10 mL vials, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520, NDC 55150-183-11
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20 de febrero de 2024 · Clase II · En curso · D-0366-2024 · Methylprednisolone acetate
Failed Dissolution Specifications
Methylprednisolone acetate Injectable Suspension, USP, 400mg per 5mL (80mg/mL, 5mL Multiple-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-314-01
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15 de febrero de 2024 · Clase I · En curso · D-0440-2024 · Methocarbamol
Presence of Particulate Matter
Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor, NJ 08520, NDC 55150-223-10
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7 de febrero de 2024 · Clase II · Cerrado por la FDA · D-0371-2024 · Rocuronium bromide
cGMP Deviations: Products were stored outside the drug label specifications.
Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10
2023
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28 de septiembre de 2023 · Clase II · En curso · D-0041-2024 · Triamcinolone acetonide
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For Intramuscular or Intra-articular use only, Shake Well, Not for IV/ID, intraocular, epidural, or intra
2022
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28 de diciembre de 2022 · Clase II · En curso · D-0095-2023 · Acyclovir
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd, E. Windsor, NJ 08520; Made in India. NDC 55150-155-20
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30 de septiembre de 2022 · Clase II · Cerrado por la FDA · D-0020-2023 · Fondaparinux sodium
Subpotent Drug: Out of specification for assay
Fondaparinux Sodium Injection, USP, 7.5 mg per 0.6 mL, Single Dose, Prefilled Syringe, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520. Made in India. NDC 55150-232-10 (carton)NDC
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26 de septiembre de 2022 · Clase II · Completado · D-0013-2023 · Acyclovir
Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Acyclovir Sodium Injection, 500mg/10mL (50mg/mL), 10 mL Single Dose Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520; Made in India, NDC 55150-154-10.
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26 de septiembre de 2022 · Clase III · En curso · D-1551-2022 · Tranexamic acid
Presence of Particulate Matter: Piece of metal found in a vial
Tranexamic Acid Injection, USP, 1000mg per 10 mL (100mg /mL), 10mL single-dose vial, Rx Only, Distributed by: AuroMedics Pharma LLC E. Windsor, NJ 08520, Made in India, NDC 55150-188-10
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13 de abril de 2022 · Clase II · Cerrado por la FDA · D-0998-2022 · Bupivacaine hydrochloride
cGMP deviations: Temperature abuse
Bupivacaine HCl Injection, single dose vial, Preservative Free 0.5%, 10mL (25/ct), Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-169-10
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13 de abril de 2022 · Clase II · Cerrado por la FDA · D-1009-2022 · Ampicillin
cGMP deviations: Temperature abuse
Ampicillin for Injection, USP, 1 g per vial, 10-count box, Rx only, Distributed by: Auromedics Pharma, NDC 55150-113-10
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13 de abril de 2022 · Clase II · Cerrado por la FDA · D-0997-2022 · Azithromycin
cGMP deviations: Temperature abuse
Azithromycin for Injection USP Vial, 500 mg per vial, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-174-10
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5 de abril de 2022 · Clase III · Cerrado por la FDA · D-0766-2022 · Cyanocobalamin
Subpotent Drug: Out of Specification results for Assay
Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx Only, Manufactured in India, for Auromedics Pharma LLC, NDC 55150-364-01.
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26 de enero de 2022 · Clase I · Cerrado por la FDA · D-0556-2022 · Polymyxin b sulfate
Presence of Particulate Matter; product complaint of hair discovered in a vial within the lot
Polymyxin B for Injection USP, 500,000 Units per Vial, 10 mL vials, packaged in 10 vials per carton, Sterile, Rx Only, Distributed by: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-234-10
2020
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30 de diciembre de 2020 · Clase II · Cerrado por la FDA · D-0248-2021 · Acetaminophen
Discoloration and failed pH specifications
Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose Vial, For Intravenous Use Only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 Made in India NDC 55150-3
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7 de febrero de 2020 · Clase III · Cerrado por la FDA · D-0853-2020 · Glycopyrrolate
Failed Impurities/Degradation Specifications: elevated levels of Benzaldehyde impurity was found in investigative samples (retain samples).
Glycopyrrolate Injection, USP 4 mg per 20 mL (0.2 mg/mL), 20 mL Multiple Dose Vial, Rx Only, For Intramuscular or Intravenous Use, Not for Use in Newborns, Contains Benzyl Alcohol, Distributed by: AuroMedics Pharma LLC,
2019
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25 de noviembre de 2019 · Clase II · Cerrado por la FDA · D-0574-2020 · Vancomycin
Discoloration: Product complaints of discoloration after reconstitution of vials.
Vancomycin Hydrochloride for Injection, USP, 1 g* per vial, packaged in 10-count vials per carton, Rx only, Mft. in India for: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-204-20.
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11 de noviembre de 2019 · Clase III · Cerrado por la FDA · D-0521-2020 · Amiodarone hydrochloride
Crystallization: Presence of visible particulate matter.
Amiodarone Hydrochloride Injection, USP, 450 mg per 9 mL (50 mg / mL), 9 mL Single Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-181-09
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11 de noviembre de 2019 · Clase III · Cerrado por la FDA · D-0520-2020 · Amiodarone hydrochloride
Crystallization: Presence of visible particulate matter.
Amiodarone Hydrochloride Injection, USP, 150 mg per 3 mL (50 mg / mL), 3 mL Single Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-180-03
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11 de noviembre de 2019 · Clase III · Cerrado por la FDA · D-0522-2020 · Amiodarone hydrochloride
Crystallization: Presence of visible particulate matter.
Amiodarone Hydrochloride Injection, USP, 900 mg per 18 mL (50 mg / mL), 18 mL Multiple Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-182-18
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11 de noviembre de 2019 · Clase II · Cerrado por la FDA · D-0573-2020 · Bupivacaine hydrochloride, Lidocaine
Presence of Foreign Substance: Foreign material found inside the vial.
Lidocaine HCl Injection, USP, 2% 100 mg/5 mL (20 mg/mL), Preservative-Free, packaged in 10 x 5 mL Single Dose Vials per carton, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ
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28 de marzo de 2019 · Clase I · Cerrado por la FDA · D-1248-2019 · Betamethasone sodium phosphate and betamethasone acetate, Bupivacaine hydrochloride, Lidocaine
Presence of Particulate Matter: One vial was found to contain a hair.
Lidocaine HCl Injection, USP 1 % 50 mg/5 mL (10 mg/mL), 5mL vial, Rx only, Mrd. in India for: AuroMedics Pharna LLC. E Windsor, NJ 08520 NDC 55150-162-05
2018
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2 de julio de 2018 · Clase I · Cerrado por la FDA · D-1030-2018 · Piperacillin and tazobactam
Presence of Particulate Matter: identified as glass and silicone material
Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial, Rx Only. Manufactured for: Auromedics Pharma LLC 6 Wheeling Road Dayton NJ 08810, Made in India. NDC 55150-120-30
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1 de mayo de 2018 · Clase I · Cerrado por la FDA · D-0926-2018 · Piperacillin and tazobactam
Presence of Particulate Matter: confirmed customer report for presence of visible particulate matter, confirmed as glass
Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, For Intravenous Use Only, Single-Dose vial, Rx Only, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ 05610. NDC 55150-120-30
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1 de mayo de 2018 · Clase I · Cerrado por la FDA · D-0866-2018 · Ampicillin sodium and sulbactam sodium
Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active ingredients.
Ampicillin and Sulbactam for Injection, USP, 3 gram*s/vial, For Intramuscular or Intravenous Use, Sterile, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ, NDC 55150-117-20.
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0706-2018 · Levetiracetam
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levetiracetam in 0.75% Sodium Chloride Injection, 1000 mg per 100 mL (10 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-247-47.
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0705-2018 · Levetiracetam
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levetiracetam in 0.82% Sodium Chloride Injection, 500 mg per 100 mL (5 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-246-47.
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0707-2018 · Levetiracetam
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levetiracetam in 0.54% Sodium Chloride Injection, 1,500 mg per 100 mL (15 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-248-47.
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0709-2018 · Levofloxacin
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levofloxacin in 5% Dextrose Injection, 750 mg Levofloxacin (5 mg/mL) in 150 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured f
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0708-2018 · Levofloxacin
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levofloxacin in 5% Dextrose Injection, 500 mg Levofloxacin (5 mg/mL) in 100 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured f
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0704-2018 · Levofloxacin
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured fo
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27 de marzo de 2018 · Clase II · Cerrado por la FDA · D-0703-2018 · Linezolid
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous Administration, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-242-
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12 de enero de 2018 · Clase I · Cerrado por la FDA · D-0574-2018 · Levofloxacin
Presence of Particulate Matter; contains visible particulate matter identified as mold.
Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 50 mL Single-Use flexible container, Rx Only, Manufactured for: AuroMedics Pharma LLC 6 Wheeling Drive, Dayton, NJ 08810 Manufactured for: Aurobindo Pharma L
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2 de enero de 2018 · Clase I · Cerrado por la FDA · D-0339-2018 · Ampicillin sodium and sulbactam sodium
Presence of Particulate Matter: A confirmed customer report was received for the presence of visible particulate matter, confirmed as glass, within a single vial.
Ampicillin and Sulbactam for Injection 1.5 g vial, sterile Dry Powder for injection, 10 vials per carton, Distributed by AuroMedics Pharma LLC. 279 Princeton-Highstown Rd. E. Windsor, NJ 08520, NDC 55150-116-20
2017
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20 de diciembre de 2017 · Clase I · Cerrado por la FDA · D-0337-2018 · Linezolid
Presence of Particulate Matter; white particulate matter identified as mold was found in one bag
Linezolid Injection 600 mg/300 mL (2 mg/mL), 300 mL Single-use, ready-to-use flexible plastic infusion bags in a foil laminate overwrap, Rx only, Mfd in India for: AuroMedics Pharma LLC, Dayton, NJ --- NDC 55150-242-51
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4 de diciembre de 2017 · Clase I · Cerrado por la FDA · D-0340-2018 · Pantoprazole sodium
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only, Manufactured in India for: AuroMedics Pharma LLC, 6 Wheeling ROad, Dayton, NJ 08810. NDC 55150-202-00
2016
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16 de diciembre de 2016 · Clase III · Cerrado por la FDA · D-0470-2017 · Pantoprazole sodium
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ 08810, NDC 55150-202-00
¿Qué significan las clases de retiro?
Clase I: El tipo más grave: existe una probabilidad razonable de que usar el producto cause problemas de salud graves o la muerte.
Clase II: Usar el producto puede causar problemas de salud temporales o reversibles con tratamiento, o la probabilidad de problemas graves es remota.
Clase III: No es probable que usar el producto cause problemas de salud (por ejemplo, un problema de etiquetado o de envase).
Siguientes pasos
- Encuentre una farmacia cerca de ustedPregunte qué empresa fabricó su medicamento y si tiene un retiro
- Últimos retiros de medicamentos de la FDATodas las empresas, los más recientes primero
- Todas las empresas farmacéuticasDe la A a la Z
- Todos los medicamentos con receta de la A a la ZBusque por nombre genérico, de marca o en español
Fuentes
- NDC Directory (openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 30 de octubre de 2026, consultados el 31 de octubre de 2026
- Drugs@FDA (openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 30 de octubre de 2026, consultados el 31 de octubre de 2026
- Drug recall enforcement reports (openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 27 de octubre de 2026, consultados el 31 de octubre de 2026
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