Drug company (FDA labeler)
Carwin Pharmaceutical Associates, LLC
NDC labeler code: 15370
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
- Potassium chlorideKlor-Con, Klor-Con M, Pokonza · 3 products
- AripiprazoleAbilify, Opipza, Abilify Asimtufii · 3 products
- DiclofenacZipsor, Lofena, Cambia · 2 products
- ClotrimazoleClotic (Clotrimazole) Otic Solution · 1 product
- NabumetoneRelafen Ds · 1 product
- Carbinoxamine maleateKarbinal ER, Carbzah, Ryvent · 1 product
- CelecoxibCelebrex, Vyscoxa, Elyxyb - Celecoxib · 1 product
- Dexchlorpheniramine maleateCorphena, Ryclora · 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 |
|---|---|---|---|
| September 26, 2025 | NDA217628 | Clotrimazole CLOTIC | Carwin Pharm Assoc |
| July 29, 2025 | NDA211759 | Celecoxib VYSCOXA | Carwin Pharm Assoc |
| July 22, 2024 | NDA216655 | Aripiprazole OPIPZA | Xiamen LP Pharm Co |
| August 30, 2019 | ANDA203166 | Nabumetone NABUMETONE | Lgm Pharma |
| July 16, 2018 | ANDA202520 | Dexchlorpheniramine maleate POLMON | Pharmobedient |
| May 31, 2016 | ANDA207484 | Carbinoxamine maleate CARBINOXAMINE MALEATE | Pharmobedient |
| August 19, 2015 | NDA208019 | Potassium chloride POKONZA, POTASSIUM CHLORIDE | Genus |
| December 22, 2014 | NDA206814 | Potassium chloride POKONZA, POTASSIUM CHLORIDE | Genus Lifesciences |
| March 18, 2004 | ANDA076561 | Diclofenac CATAFLAM | Pangea |
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.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
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- All prescription drugs A to ZSearch by generic, brand or Spanish name
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