FDA NDC Directory · JSON-LD · Markdown
NDC 72789-049 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE
| Labeler / Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA207138 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | OXYBUTYNIN CHLORIDE (10 mg/1) |
| Marketing started | 20161220 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).