NDC 68382-987
Solifenacin
Solifenacin
Solifenacin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals Usa Inc.. The primary component is Solifenacin Succinate.
| Product ID | 68382-987_a91df415-ca99-476a-b7b7-11e5d2c169db |
| NDC | 68382-987 |
| 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 Pharmaceuticals USA Inc. |
| 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 |