OXYBUTYNIN CHLORIDE
- Product NDC
- 68071-4395
- 11-digit product format
- 680714395
- Labeler code
- 68071
- Product ID
- 68071-4395_7bacbd38-1be4-1a0d-e053-2991aa0a07dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209025
- Marketing category
- ANDA
- Marketing start
- 2018-02-01
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record