Solifenacin Succinate 00591-3795
Product NDC
00591-3795- Manufacturer
- Actavis Pharma, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 30, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA202551
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Solifenacin Succinate | 5 mg/1 |
Drug Class
Cholinergic Muscarinic Antagonist [EPC]Cholinergic Muscarinic Antagonists [MoA]
Packaging Options(2)
90 TABLET, FILM COATED in 1 BOTTLE (0591-3795-19)
30 TABLET, FILM COATED in 1 BOTTLE (0591-3795-30)