Oxybutynin 70771-1088
Product NDC
70771-1088- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 10, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA202332
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxybutynin Chloride | 15 mg/1 |
Drug Class
Cholinergic Muscarinic Antagonist [EPC]Cholinergic Muscarinic Antagonists [MoA]
Packaging Options(6)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-1)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-3)
10 BLISTER PACK in 1 CARTON (70771-1088-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1088-2)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-5)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-6)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1088-9)