FDA NDC Directory · JSON-LD · Markdown
NDC 85509-1001 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | PHOENIX RX LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078722 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | CYCLOBENZAPRINE HYDROCHLORIDE (7.5 mg/1) |
| Marketing started | 20150325 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).