Oxybutynin Chloride 72189-0132
Product NDC
72189-0132- Manufacturer
- Direct Rx
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 24, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA207138
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxybutynin Chloride | 10 mg/1 |
Drug Class
Cholinergic Muscarinic Antagonist [EPC]Cholinergic Muscarinic Antagonists [MoA]
Packaging Options(1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)