Oxybutynin Chloride
- Product NDC
- 43063-145
- 11-digit product format
- 430630145
- Labeler code
- 43063
- Product ID
- 43063-145_7d3ab634-7cad-36af-e053-2a91aa0af8e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075079
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- 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