Package 63629-8868-1

Brand: solifenacin succinate

Generic: solifenacin succinate
NDC Package

Package Facts

Identity

Package NDC 63629-8868-1
Digits Only 6362988681
Product NDC 63629-8868
Product ID 63629-8868_43806415-3afe-452f-8c9f-3f029c0f82ca
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-8868-1)

Marketing

Marketing Status
Marketed Since 2021-09-30
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": "43806415-3afe-452f-8c9f-3f029c0f82ca", "openfda": {"unii": ["KKA5DLD701"], "rxcui": ["477367"], "spl_set_id": ["8d65dcb9-aa67-4cfb-9d15-43d0de327bd7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-8868-1)", "package_ndc": "63629-8868-1", "marketing_start_date": "20210930"}], "brand_name": "Solifenacin Succinate", "product_id": "63629-8868_43806415-3afe-452f-8c9f-3f029c0f82ca", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "63629-8868", "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": "ANDA210224", "marketing_category": "ANDA", "marketing_start_date": "20190521", "listing_expiration_date": "20261231"}