OXYBUTYNIN CHLORIDE
- Product NDC
- 50090-7766
- 11-digit product format
- 500907766
- Labeler code
- 50090
- Product ID
- 50090-7766_495472e9-88f2-4df2-b2e9-f3c5b5806cd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209025
- Marketing category
- ANDA
- Marketing start
- 2018-02-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L9F3D9RENQ | OXYBUTYNIN CHLORIDE | 1508-65-2 | OXYBUTYNIN CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7766-0 | 50090776600 | 90 TABLET in 1 BOTTLE (50090-7766-0) | 90 tablet | 2025-11-12 | No | No | Historical |