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NDC 0615-8220 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Labeler / Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA202332 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | OXYBUTYNIN CHLORIDE (10 mg/1) |
| Marketing started | 20170810 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).