NDC 70771-1604
Solifenacin
Solifenacin
Solifenacin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Zydus Lifesciences Limited. The primary component is Solifenacin Succinate.
| Product ID | 70771-1604_205b6c54-6d0b-4c07-b4b8-7a95e9456282 |
| NDC | 70771-1604 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Solifenacin |
| Generic Name | Solifenacin |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-02-10 |
| Marketing Category | ANDA / |
| Application Number | ANDA207721 |
| Labeler Name | Zydus Lifesciences Limited |
| Substance Name | SOLIFENACIN SUCCINATE |
| Active Ingredient Strength | 5 mg/1 |
| Pharm Classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |