Ursodiol 70710-1128
Product NDC
70710-1128- Manufacturer
- Zydus Pharmaceuticals (usa) Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 7, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA211145
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ursodiol | 500 mg/1 |
Drug Class
Bile Acid [EPC]Bile Acid [EPC]Bile Acids and Salts [CS]
Packaging Options(2)
100 TABLET in 1 BOTTLE (70710-1128-1)
500 TABLET in 1 BOTTLE (70710-1128-5)