FDA NDC Directory · JSON-LD · Markdown
NDC 72189-129 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | losartan potassium and hydrochlorothiazide |
|---|---|
| Labeler / Manufacturer | Direct_Rx |
| Marketing category | Abbreviated NDA (generic) · App ANDA201845 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | HYDROCHLOROTHIAZIDE (12.5 mg/1) LOSARTAN POTASSIUM (50 mg/1) |
| Marketing started | 20201015 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).