Oxybutynin Chloride 72789-0417
Product NDC
72789-0417- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA209025
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxybutynin Chloride | 5 mg/1 |
Drug Class
Cholinergic Muscarinic Antagonist [EPC]Cholinergic Muscarinic Antagonists [MoA]
Packaging Options(2)
30 TABLET in 1 BOTTLE, PLASTIC (72789-417-30)
90 TABLET in 1 BOTTLE, PLASTIC (72789-417-90)