Details for New Drug Application (NDA): 215761
✉ Email this page to a colleague
NDA 215761 describes SOLIFENACIN SUCCINATE, which is a drug marketed by Accord Hlthcare, Ajanta Pharma Ltd, Alembic, Alkem Labs Ltd, Amneal Pharms Co, Annora Pharma, Aurobindo Pharma, Bostal, Breckenridge, Chartwell Rx, Cipla, Glenmark Speclt, Jubilant Generics, Lannett Co Inc, Macleods Pharms Ltd, MSN, Novitium Pharma, Qilu, Rising, Sciegen Pharms, Sunshine, Teva Pharms Usa, Torrent, Unichem, Watson Labs Inc, and Zydus Pharms, and is included in twenty-six NDAs. It is available from nineteen suppliers. Additional details are available on the SOLIFENACIN SUCCINATE profile page.
The generic ingredient in SOLIFENACIN SUCCINATE is solifenacin succinate. There are thirty drug master file entries for this compound. Twenty suppliers are listed for this compound. Additional details are available on the solifenacin succinate profile page.
The generic ingredient in SOLIFENACIN SUCCINATE is solifenacin succinate. There are thirty drug master file entries for this compound. Twenty suppliers are listed for this compound. Additional details are available on the solifenacin succinate profile page.
Summary for 215761
| Tradename: | SOLIFENACIN SUCCINATE |
| Applicant: | Annora Pharma |
| Ingredient: | solifenacin succinate |
| Patents: | 0 |
Pharmacology for NDA: 215761
| Mechanism of Action | Cholinergic Muscarinic Antagonists |
Medical Subject Heading (MeSH) Categories for 215761
Suppliers and Packaging for NDA: 215761
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SOLIFENACIN SUCCINATE | solifenacin succinate | TABLET;ORAL | 215761 | ANDA | Camber Pharmaceuticals, Inc. | 31722-027 | 31722-027-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-027-30) |
| SOLIFENACIN SUCCINATE | solifenacin succinate | TABLET;ORAL | 215761 | ANDA | Camber Pharmaceuticals, Inc. | 31722-027 | 31722-027-31 | 10 BLISTER PACK in 1 CARTON (31722-027-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-027-32) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | Jun 15, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Jun 15, 2022 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
