Drug company (FDA labeler)
Kesin Pharma Corporation
NDC labeler code: 81033
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.
Prescription medicines
- ValsartanDiovan · 4 products
- GabapentinNeurontin, Gralise, Relgaabi · 3 products
- Potassium chlorideKlor-Con, Klor-Con M, Pokonza · 3 products
- NystatinNystop, Klayesta, Nyamyc · 2 products
- LactuloseKristalose, Lactulose Crystalline, Enulose · 2 products
- AtorvastatinLipitor · 2 products
- MupirocinPirnuo · 1 product
- Megestrol acetate1 product
- AtovaquoneMepron · 1 product
- SucralfateCarafate · 1 product
- LacosamideVimpat, Motpoly XR · 1 product
- Promethazine hydrochloridePhenergan, Promethegan · 1 product
- Valproic acid1 product
- Chlorhexidine gluconatePeriogard Alcohol Free, Dash Chlorhexidine Gluconate 0.12% Oral Rinse, Chlorhexidine Gluconate 0.12% Oral Rinse · 1 product
- FamotidinePepcid · 1 product
- FosfomycinContepo · 1 product
- MetronidazoleMetronidazole Vaginal, Metronidazole Vaginal Gel, Likmez · 1 product
- DexamethasoneTaperdex 6-Day, Hemady, Taperdex 12-Day · 1 product
- LevetiracetamKeppra, Spritam, Keppra XR · 1 product
- LidocaineXylocaine Mpf, Xylocaine, Lidocaine Viscous · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| June 26, 2025 | ANDA219699 | Lacosamide LACOSAMIDE | Ajenat Pharms |
| May 21, 2024 | ANDA216474 | Sucralfate SUCRALFATE | Strides Pharma |
| September 22, 2023 | NDA216755 | Metronidazole LIKMEZ | Saptalis Pharms |
| July 7, 2023 | ANDA217137 | Famotidine FAMOTIDINE | Carnegie |
| October 21, 2021 | ANDA214554 | Fosfomycin FOSFOMYCIN TROMETHAMINE | Alkem Labs Ltd |
| May 21, 2021 | ANDA211648 | Potassium chloride POTASSIUM CHLORIDE | Sciegen Pharms |
| April 20, 2021 | ANDA212695 | Lidocaine LIDOCAINE | Quagen |
| March 11, 2021 | ANDA211667 | Potassium chloride POTASSIUM CHLORIDE | Strides Pharma |
| May 31, 2019 | ANDA210510 | Atovaquone ATOVAQUONE | Abhai LLC |
| March 12, 2019 | ANDA205536 | Valsartan VALSARTAN | Alkem Labs Ltd |
| December 21, 2018 | ANDA209288 | Atorvastatin ATORVASTATIN CALCIUM | Alkem Labs Ltd |
| March 14, 2016 | ANDA091286 | Gabapentin GABAPENTIN | Ajenat Pharms |
| March 13, 2009 | ANDA040891 | Promethazine hydrochloride PROMETHAZINE HYDROCHLORIDE | Strides Pharma |
| January 16, 2009 | ANDA079120 | Levetiracetam LEVETIRACETAM | Bionpharma |
| November 7, 2003 | ANDA065123 | Mupirocin MUPIROCIN | Padagis Israel |
| July 28, 2003 | ANDA076645 | Lactulose LACTULOSE | Bajaj |
| July 25, 2001 | ANDA075671 | Megestrol acetate MEGESTROL ACETATE | Strides Pharma Intl |
| November 14, 2000 | ANDA075561 | Chlorhexidine gluconate CHLORHEXIDINE GLUCONATE | Bajaj |
| August 25, 1992 | ANDA073178 | Valproic acid VALPROIC ACID | Ani Pharms |
| December 27, 1991 | ANDA062832 | Nystatin NYSTATIN | Sciegen Pharms |
| September 21, 1976 | ANDA084754 | Dexamethasone DEXAMETHASONE | Pharmazone |
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
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026