FDA NDC Directory · JSON-LD · Markdown
NDC 0121-1019 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA090622 |
| Dosage form / route | TABLET · SUBLINGUAL |
| Active ingredients | BUPRENORPHINE HYDROCHLORIDE (2 mg/1) |
| Marketing started | 20231012 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).