← FDA Drug Approvals (Drugs@FDA)
OXYBUTYNIN CHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: UNIQUE · Approved 2016-05-27
Drug application
- FDA Application #
ANDA206121- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- OXYBUTYNIN CHLORIDE
- Generic name
- OXYBUTYNIN CHLORIDE
- Active ingredients
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- UNIQUE
- Manufacturer
- Rising Pharma Holdings, Inc.
- First approval
- 2016-05-27
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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