Drug company (FDA labeler)
IPG Pharmaceuticals, Inc.
NDC labeler code: 71085
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
- BuspironeBucapsol · 2 products
- KetoconazoleKetodan · 1 product
- Potassium chlorideKlor-Con, Klor-Con M, Pokonza · 1 product
- TofacitinibXeljanz, Xeljanz XR · 1 product
- Lidocaine and tetracainePliaglis · 1 product
- Carbinoxamine maleateKarbinal ER, Carbzah, Ryvent · 1 product
- Clemastine fumarateClemsza · 1 product
- FlurbiprofenLurbiro · 1 product
- Fluticasone propionateFluticasone Propionate Diskus, Xhance, Flovent Diskus · 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 9, 2026 | ANDA219370 | Tofacitinib TOFACITINIB CITRATE | Pharmaco |
| April 16, 2019 | ANDA208972 | Buspirone BUSPIRONE HYDROCHLORIDE | Epic Pharma LLC |
| August 19, 2015 | NDA208019 | Potassium chloride POKONZA, POTASSIUM CHLORIDE | Genus |
| September 12, 2007 | ANDA077538 | Fluticasone propionate FLUTICASONE PROPIONATE | Apotex |
| June 29, 2006 | NDA021717 | Lidocaine and tetracaine PLIAGLIS | Crescita Therap |
| April 25, 2003 | ANDA040458 | Carbinoxamine maleate CARBINOXAMINE MALEATE | Genus |
| December 18, 2002 | ANDA075638 | Ketoconazole KETOZOLE | Sun Pharma Canada |
| May 31, 1995 | ANDA074431 | Flurbiprofen FLURBIPROFEN | Genus |
| January 31, 1992 | ANDA073283 | Clemastine fumarate CLEMASTINE FUMARATE | Genus |
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
- All drug companiesA to Z
- 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