OXYBUTYNIN CHLORIDE
- Product NDC
- 0179-0187
- 11-digit product format
- 001790187
- Labeler code
- 0179
- Product ID
- 0179-0187_7bea8f7b-5283-26f9-e053-2991aa0afaec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA076745
- Marketing category
- ANDA
- Marketing start
- 2015-10-14
- Marketing end
- 2020-06-30
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record