OXYBUTYNIN CHLORIDE
- Product NDC
- 70518-1294
- 11-digit product format
- 705181294
- Labeler code
- 70518
- Product ID
- 70518-1294_922cac62-3797-71e9-e053-2a95a90a8e2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209025
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- 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