Ursodiol 00904-6890
Product NDC
00904-6890- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 1, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA202540
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ursodiol | 250 mg/1 |
Drug Class
Bile Acid [EPC]Bile Acid [EPC]Bile Acids and Salts [CS]
Packaging Options(1)
30 BLISTER PACK in 1 CARTON (0904-6890-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK