Drug company (FDA labeler)
Ipca Laboratories Limited
NDC labeler code: 83980
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
- Propranolol hydrochlorideInderal La, Inderal XL, Hemangeol · 5 products
- Ondansetron4 products
- Etodolac4 products
- FurosemideLasix, Furoscix, Lasix Onyu · 3 products
- AtenololTenormin · 3 products
- MetoclopramideReglan, Gimoti · 2 products
- ChlorthalidoneThalitone, Hemiclor · 2 products
- Hydroxychloroquine sulfatePlaquenil, Sovuna · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| November 12, 2024 | ANDA209162 | Chlorthalidone CHLORTHALIDONE | Ipca Labs Ltd |
| August 1, 2024 | ANDA205448 | Etodolac ETODOLAC | Ipca Labs Ltd |
| May 1, 2024 | ANDA204729 | Etodolac ETODOLAC | Ipca Labs Ltd |
| October 30, 2023 | ANDA209389 | Ondansetron ONDANSETRON | Ipca Labs Ltd |
| January 23, 2014 | ANDA203761 | Ondansetron ONDANSETRON HYDROCHLORIDE | Ipca Labs Ltd |
| June 12, 2008 | ANDA078807 | Metoclopramide METOCLOPRAMIDE HYDROCHLORIDE | Ipca Labs Ltd |
| June 2, 2008 | ANDA078955 | Propranolol hydrochloride PROPRANOLOL HYDROCHLORIDE | Ipca Labs Ltd |
| June 14, 2007 | ANDA040766 | Hydroxychloroquine sulfate HYDROXYCHLOROQUINE SULFATE | Ipca Labs Ltd |
| December 27, 2006 | ANDA077877 | Atenolol ATENOLOL | Ipca Labs Ltd |
| September 18, 2006 | ANDA078010 | Furosemide FUROSEMIDE | Ipca Labs Ltd |
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