FDA NDC Directory · JSON-LD · Markdown
NDC 43547-381 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Generic name | Duloxetine |
|---|---|
| Labeler / Manufacturer | Solco Healthcare US, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA206653 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | DULOXETINE HYDROCHLORIDE (60 mg/1) |
| Marketing started | 20160120 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).