Details for New Drug Application (NDA): 207721
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The generic ingredient in SOLIFENACIN SUCCINATE is solifenacin succinate. There are thirty drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the solifenacin succinate profile page.
Summary for 207721
Tradename: | SOLIFENACIN SUCCINATE |
Applicant: | Zydus Pharms |
Ingredient: | solifenacin succinate |
Patents: | 0 |
Pharmacology for NDA: 207721
Mechanism of Action | Cholinergic Muscarinic Antagonists |
Medical Subject Heading (MeSH) Categories for 207721
Suppliers and Packaging for NDA: 207721
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
SOLIFENACIN SUCCINATE | solifenacin succinate | TABLET;ORAL | 207721 | ANDA | Zydus Pharmaceuticals USA Inc. | 68382-987 | 68382-987-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-987-06) |
SOLIFENACIN SUCCINATE | solifenacin succinate | TABLET;ORAL | 207721 | ANDA | Zydus Pharmaceuticals USA Inc. | 68382-987 | 68382-987-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-987-16) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Oct 19, 2020 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Oct 19, 2020 | TE: | RLD: | No |
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