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NDC 60505-4379 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | paroxetine hydrochloride |
|---|---|
| Labeler / Manufacturer | Apotex Corp |
| Marketing category | New Drug Application (innovator) · App NDA020936 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | PAROXETINE HYDROCHLORIDE (37.5 mg/1) |
| Marketing started | 20110101 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).