solifenacin succinate

Generic: solifenacin succinate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name solifenacin succinate
Generic Name solifenacin succinate
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

solifenacin succinate 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-561
Product ID 71205-561_a3a77fb3-af3f-4c6f-be7e-8ce349d2a2cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210224
Listing Expiration 2026-12-31
Marketing Start 2019-05-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205561
Hyphenated Format 71205-561

Supplemental Identifiers

RxCUI
477367
UPC
0371205561307
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 ANDA210224 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-561-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-561-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-561-90)
source: ndc

Packages (3)

71205-561-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-561-30) 71205-561-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-561-60) 71205-561-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-561-90)

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": "a3a77fb3-af3f-4c6f-be7e-8ce349d2a2cc", "openfda": {"upc": ["0371205561307"], "unii": ["KKA5DLD701"], "rxcui": ["477367"], "spl_set_id": ["c67107f4-348b-4a23-a67c-26fd8241ebd6"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-561-30)", "package_ndc": "71205-561-30", "marketing_start_date": "20210507"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-561-60)", "package_ndc": "71205-561-60", "marketing_start_date": "20210507"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-561-90)", "package_ndc": "71205-561-90", "marketing_start_date": "20210507"}], "brand_name": "Solifenacin Succinate", "product_id": "71205-561_a3a77fb3-af3f-4c6f-be7e-8ce349d2a2cc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71205-561", "generic_name": "Solifenacin Succinate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solifenacin Succinate", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "5 mg/1"}], "application_number": "ANDA210224", "marketing_category": "ANDA", "marketing_start_date": "20190521", "listing_expiration_date": "20261231"}