FDA NDC Directory · JSON-LD · Markdown
NDC 0777-3105 · HUMAN PRESCRIPTION DRUG · CAPSULE
| Generic name | Fluoxetine hydrochloride |
|---|---|
| Labeler / Manufacturer | Dista Products Company |
| Marketing category | New Drug Application (innovator) · App NDA018936 |
| Dosage form / route | CAPSULE · ORAL |
| Active ingredients | FLUOXETINE HYDROCHLORIDE (20 mg/1) |
| Marketing started | 19880201 |
| Marketing ended | 20270616 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).