FDA NDC Directory · JSON-LD · Markdown
NDC 42571-111 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | losartan potassium |
|---|---|
| Labeler / Manufacturer | Micro Labs Limited |
| Marketing category | Abbreviated NDA (generic) · App ANDA091541 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | LOSARTAN POTASSIUM (50 mg/1) |
| Marketing started | 20121206 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).