OXYBUTYNIN CHLORIDE
- Product NDC
- 50090-6199
- 11-digit product format
- 500906199
- Labeler code
- 50090
- Product ID
- 50090-6199_ace59398-ff81-4474-9740-05c8594b28ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212798
- Marketing category
- ANDA
- Marketing start
- 2019-11-01
- 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 |
|---|
| 50090-6199-0 | 50090619900 | 30 TABLET in 1 BOTTLE (50090-6199-0) | 30 tablet | 2022-11-02 | No | No | Historical |
| 50090-6199-1 | 50090619901 | 100 TABLET in 1 BOTTLE (50090-6199-1) | 100 tablet | 2022-11-02 | No | No | Historical |
| 50090-6199-3 | 50090619903 | 90 TABLET in 1 BOTTLE (50090-6199-3) | 90 tablet | 2022-11-02 | No | No | Historical |