Package 63629-8532-1

Brand: solifenacin succinate

Generic: solifenacin succinate
NDC Package

Package Facts

Identity

Package NDC 63629-8532-1
Digits Only 6362985321
Product NDC 63629-8532
Product ID 63629-8532_f1a70279-30d4-4c00-a28e-4434b85d5ced
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-8532-1)

Marketing

Marketing Status
Marketed Since 2021-05-19
Brand solifenacin succinate
Generic solifenacin succinate
Sample Package No

Linked Drug Pages (1)

SOLIFENACIN SUCCINATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1a70279-30d4-4c00-a28e-4434b85d5ced", "openfda": {"unii": ["KKA5DLD701"], "rxcui": ["477367"], "spl_set_id": ["49346a96-3d96-4702-b96e-94e635510dba"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-8532-1)", "package_ndc": "63629-8532-1", "marketing_start_date": "20210519"}], "brand_name": "SOLIFENACIN SUCCINATE", "product_id": "63629-8532_f1a70279-30d4-4c00-a28e-4434b85d5ced", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "63629-8532", "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"}