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Drug company (FDA labeler)

Unit Dose Solutions, Inc.

NDC labeler code: 87441

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

85Products (NDC)

Prescription medicines

FDA applications for these products

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
August 8, 2024ANDA218988 Trazodone hydrochloride
TRAZODONE HYDROCHLORIDE
Granules
March 31, 2023ANDA213052 Prazosin hydrochloride
PRAZOSIN HYDROCHLORIDE
Aurobindo Pharma Ltd
February 2, 2022ANDA215568 Bupropion
BUPROPION HYDROCHLORIDE
Granules
June 24, 2020ANDA213386 Prednisone
PREDNISONE
Amneal
May 8, 2020ANDA213794 Ibuprofen
IBUPROFEN
Aurobindo Pharma Ltd
March 30, 2020ANDA205601 Buprenorphine and naloxone
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE
Rhodes Pharms
November 14, 2019ANDA210907 Buspirone
BUSPIRONE HYDROCHLORIDE
Unichem
May 7, 2018ANDA209312 Methocarbamol
METHOCARBAMOL
Granules
December 13, 2017ANDA207000 Buprenorphine and naloxone
BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE
Specgx LLC
May 31, 2017ANDA208170 Cyclobenzaprine hydrochloride
CYCLOBENZAPRINE HYDROCHLORIDE
Rubicon Research
March 27, 2017ANDA207276 Buprenorphine
BUPRENORPHINE HYDROCHLORIDE
Rhodes Pharms
September 12, 2016ANDA206174 Aripiprazole
ARIPIPRAZOLE
Ajanta Pharma Ltd
December 22, 2015ANDA206530 Famotidine
FAMOTIDINE
Aurobindo Pharma Ltd
September 15, 2015ANDA091625 Ibuprofen
IBUPROFEN
Granules
October 31, 2014ANDA091672 Omeprazole
OMEPRAZOLE
Glenmark Pharms Ltd
August 20, 2014ANDA204279 Hydroxyzine
HYDROXYZINE HYDROCHLORIDE
Heritage
February 7, 2014ANDA078888 Buspirone
BUSPIRONE HYDROCHLORIDE
Zydus Pharms
September 28, 2012ANDA202038 Pantoprazole sodium
PANTOPRAZOLE SODIUM
Aurobindo Pharma Ltd
May 29, 2012ANDA090548 Atorvastatin
ATORVASTATIN CALCIUM
Apotex Inc
April 23, 2012ANDA076255 Olanzapine
OLANZAPINE
DR Reddys Labs Ltd
March 27, 2012ANDA201109 Quetiapine
QUETIAPINE FUMARATE
Lupin Ltd
June 6, 2011ANDA091497 Losartan potassium
LOSARTAN POTASSIUM
Prinston Inc
April 5, 2011ANDA079163 Divalproex sodium
DIVALPROEX SODIUM
Unichem Labs Ltd
December 17, 2010ANDA090858 Gabapentin
GABAPENTIN
Alkem
October 6, 2010ANDA090083 Losartan potassium
LOSARTAN POTASSIUM
Aurobindo Pharma
April 22, 2010ANDA090564 Metformin hydrochloride
METFORMIN HYDROCHLORIDE
Granules India
February 16, 2010ANDA090624 Sulfamethoxazole and trimethoprim
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Aurobindo Pharma
November 6, 2009ANDA090200 Methocarbamol
METHOCARBAMOL
Hetero Labs Ltd III
May 4, 2009ANDA078925 Amlodipine
AMLODIPINE BESYLATE
Alkem
March 27, 2009ANDA077627 Topiramate
TOPIRAMATE
Glenmark Pharms Ltd
January 15, 2009ANDA078993 Levetiracetam
LEVETIRACETAM
Aurobindo Pharma
January 12, 2009ANDA040796 Folic acid
FOLIC ACID
Leading
August 15, 2008ANDA040907 Hydrochlorothiazide
HYDROCHLOROTHIAZIDE
Unichem
January 31, 2008ANDA078619 Fluoxetine
FLUOXETINE HYDROCHLORIDE
Aurobindo Pharma
November 29, 2007ANDA077580 Haloperidol
HALOPERIDOL
Zydus Pharms USA
August 27, 2007ANDA040715 Benztropine mesylate
BENZTROPINE MESYLATE
Ph Health
July 31, 2007ANDA078539 Ondansetron
ONDANSETRON HYDROCHLORIDE
Aurobindo Pharma
July 25, 2007ANDA078428 Gabapentin
GABAPENTIN
Amneal Pharms Ny
March 28, 2007ANDA078250 Naproxen
NAPROXEN
Glenmark Pharms Ltd
February 6, 2007ANDA077206 Sertraline hydrochloride
SERTRALINE HYDROCHLORIDE
Aurobindo Pharma
February 6, 2007ANDA077670 Sertraline hydrochloride
SERTRALINE HYDROCHLORIDE
Lupin
August 18, 2006ANDA077662 Gabapentin
GABAPENTIN
Glenmark Pharms Ltd
November 18, 2005ANDA040596 Promethazine hydrochloride
PROMETHAZINE HYDROCHLORIDE
Zydus Pharms USA
November 9, 2005ANDA077293 Furosemide
FUROSEMIDE
Leading
September 9, 2005ANDA077321 Lisinopril
LISINOPRIL
Lupin
October 22, 2004ANDA076921 Mirtazapine
MIRTAZAPINE
Aurobindo
June 20, 2002ANDA076003 Tramadol hydrochloride
TRAMADOL HYDROCHLORIDE
Amneal Pharms
May 31, 2001ANDA040419 Acetaminophen and codeine phosphate
ACETAMINOPHEN AND CODEINE PHOSPHATE
Specgx LLC
February 2, 2001ANDA065061 Clindamycin
CLINDAMYCIN HYDROCHLORIDE
Sun Pharm Inds Ltd
October 6, 2000ANDA075468 Clonazepam
CLONAZEPAM
Rubicon Research
September 7, 1999ANDA040317 Dicyclomine hydrochloride
DICYCLOMINE HYDROCHLORIDE
Aurobindo Pharma USA
September 10, 1996ANDA074569 Clonazepam
CLONAZEPAM
Teva
October 31, 1991ANDA072926 Lorazepam
LORAZEPAM
Watson Labs
October 31, 1991ANDA072927 Lorazepam
LORAZEPAM
Watson Labs
October 31, 1991ANDA072928 Lorazepam
LORAZEPAM
Watson Labs
December 11, 1987ANDA071523 Trazodone hydrochloride
TRAZODONE HYDROCHLORIDE
Teva Pharms USA
September 4, 1987ANDA070923 Clonidine
CLONIDINE HYDROCHLORIDE
Tp Anda Holdings
February 13, 1987ANDA062702 Cephalexin
CEPHALEXIN
Teva
December 16, 1986ANDA070975 Clonidine
CLONIDINE HYDROCHLORIDE
Actavis Elizabeth
September 4, 1985ANDA070325 Diazepam
DIAZEPAM
Mylan
November 7, 1984ANDA062396 Doxycycline
DOXYCYCLINE HYCLATE
Hikma
December 14, 1981ANDA086183 Hydroxyzine
HYDROXYZINE PAMOATE
Sandoz
December 14, 1981ANDA087479 Hydroxyzine
HYDROXYZINE PAMOATE
Sandoz
June 10, 1976ANDA084769 Chlordiazepoxide hydrochloride
CHLORDIAZEPOXIDE HYDROCHLORIDE
Barr

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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