solifenacin succinate

Generic: solifenacin succinate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name solifenacin succinate
Generic Name solifenacin succinate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

solifenacin succinate 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2423
Product ID 71335-2423_615305a0-25db-4e41-a63c-d00d0f5abd95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211657
Listing Expiration 2026-12-31
Marketing Start 2019-05-20

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352423
Hyphenated Format 71335-2423

Supplemental Identifiers

RxCUI
477367
UNII
KKA5DLD701

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name solifenacin succinate (source: ndc)
Generic Name solifenacin succinate (source: ndc)
Application Number ANDA211657 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2423-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-2423-2)
source: ndc

Packages (2)

71335-2423-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2423-1) 71335-2423-2 90 TABLET, FILM COATED in 1 BOTTLE (71335-2423-2)

Ingredients (1)

solifenacin succinate (5 mg/1)

Linked Drug Pages (1)

SOLIFENACIN SUCCINATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "615305a0-25db-4e41-a63c-d00d0f5abd95", "openfda": {"unii": ["KKA5DLD701"], "rxcui": ["477367"], "spl_set_id": ["7eb1a5d6-4972-44f4-8ab9-80b932bf81e0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2423-1)", "package_ndc": "71335-2423-1", "marketing_start_date": "20240701"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2423-2)", "package_ndc": "71335-2423-2", "marketing_start_date": "20240701"}], "brand_name": "SOLIFENACIN SUCCINATE", "product_id": "71335-2423_615305a0-25db-4e41-a63c-d00d0f5abd95", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71335-2423", "generic_name": "SOLIFENACIN SUCCINATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLIFENACIN SUCCINATE", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "5 mg/1"}], "application_number": "ANDA211657", "marketing_category": "ANDA", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}