Oxybutynin Chloride
- Product NDC
- 50090-0317
- 11-digit product format
- 500900317
- Labeler code
- 50090
- Product ID
- 50090-0317_668cabca-35a6-4b47-b356-c6b077a8c0b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074625
- Marketing category
- ANDA
- Marketing start
- 2011-11-07
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record