Drug company (FDA labeler)
INA Pharmaceutics Inc
NDC labeler code: 74157
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
- GabapentinNeurontin, Gralise, Relgaabi · 2 products
- DiflunisalDolobid · 2 products
- FlurandrenolideCordran · 2 products
- Prednisone2 products
- DiclofenacZipsor, Lofena, Cambia · 2 products
- HalcinonideHalog · 1 product
- Amcinonide1 product
- DesloratadineClarinex · 1 product
- Clobetasol propionateClobetasol Propionate (Emollient), Byqlovi, Tovet (Emollient Formulation) · 1 product
- Metaxalone1 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 |
|---|---|---|---|
| October 1, 2025 | ANDA219477 | Prednisone PREDNISONE | DR Reddys |
| May 29, 2024 | ANDA217671 | Halcinonide HALCINONIDE | Encube |
| March 4, 2024 | ANDA211313 | Gabapentin GABAPENTIN | Strides Pharma |
| March 15, 2023 | ANDA215787 | Diclofenac DICLOFENAC POTASSIUM | Pharmazone |
| November 28, 2017 | NDA209483 | Clobetasol propionate IMPOYZ | Primus Pharms |
| May 26, 2016 | ANDA202936 | Desloratadine DESLORATADINE | Taro |
| June 1, 2015 | NDA022503 | Metaxalone METAXALONE | Primus Pharms |
| March 8, 2012 | ANDA202845 | Diflunisal DIFLUNISAL | Heritage Pharma |
| May 31, 2002 | ANDA076229 | Amcinonide AMCINONIDE | Taro Pharm Inds |
| November 20, 1998 | ANDA075229 | Diclofenac DICLOFENAC POTASSIUM | Rubicon Research |
| October 18, 1965 | NDA012806 | Flurandrenolide CORDRAN, CORDRAN SP | Ina Pharms |
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