Oxybutynin Chloride
- Product NDC
- 71335-2330
- 11-digit product format
- 713352330
- Labeler code
- 71335
- Product ID
- 71335-2330_f17867c4-736e-4bde-be54-68ba1903a686
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206121
- Marketing category
- ANDA
- Marketing start
- 2016-09-27
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2330-1 | 71335233001 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2330-1) | 2024-01-18 | No | No | Historical |
| 71335-2330-2 | 71335233002 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2330-2) | 2024-01-18 | No | No | Historical |