← FDA Drug Approvals (Drugs@FDA)
OXYBUTYNIN CHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA · Approved 1988-11-14
Drug application
- FDA Application #
ANDA071655- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- OXYBUTYNIN CHLORIDE
- Generic name
- OXYBUTYNIN CHLORIDE
- Active ingredients
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- TEVA PHARMS USA
- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- First approval
- 1988-11-14
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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