FDA NDC Directory · JSON-LD · Markdown
NDC 80725-809 · HUMAN PRESCRIPTION DRUG · CAPSULE
| Generic name | DUTASTERIDE and TAMSULOSIN HYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | Waylis Therapeutics |
| Marketing category | New Drug Application (innovator) · App NDA022460 |
| Dosage form / route | CAPSULE · ORAL |
| Active ingredients | DUTASTERIDE (.5 mg/1) TAMSULOSIN HYDROCHLORIDE (.4 mg/1) |
| Marketing started | 20240301 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).