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Last Updated: November 21, 2024

Details for New Drug Application (NDA): 215761


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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, Austarpharma, Breckenridge, Chartwell Rx, Cipla, Glenmark Speclt, Jubilant Generics, Lannett Co Inc, Macleods Pharms Ltd, MSN, Qilu, Rising, Sciegen Pharms Inc, Strides Pharma, Sunshine, Teva Pharms Usa, Unichem, Watson Labs Inc, and Zydus Pharms, and is included in twenty-five NDAs. It is available from twenty-six 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-seven 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
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:RXDosage:TABLET;ORALStrength5MG
Approval Date:Jun 15, 2022TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:Jun 15, 2022TE:ABRLD:No

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