oxybutynin
- Product NDC
- 70518-2331
- 11-digit product format
- 705182331
- Labeler code
- 70518
- Product ID
- 70518-2331_93ced2f0-ebb2-02f7-e053-2a95a90a59be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202332
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record