FDA NDC Directory · JSON-LD · Markdown
NDC 51655-237 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Labeler / Manufacturer | Northwind Health Company, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA208706 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | DULOXETINE HYDROCHLORIDE (60 mg/1) |
| Marketing started | 20210423 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).