FDA NDC Directory · JSON-LD · Markdown
NDC 43598-632 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Dr. Reddy's Laboratories Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA211721 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FLUOXETINE HYDROCHLORIDE (60 mg/1) |
| Marketing started | 20190128 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).