Package 63629-8869-1

Brand: solifenacin succinate

Generic: solifenacin succinate
NDC Package

Package Facts

Identity

Package NDC 63629-8869-1
Digits Only 6362988691
Product NDC 63629-8869
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-8869-1)

Marketing

Marketing Status
Marketed Since 2021-09-30
Brand solifenacin succinate
Generic solifenacin succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc62246b-3427-4e5a-9d12-91ecfd2bb342", "openfda": {"unii": ["KKA5DLD701"], "rxcui": ["477372"], "spl_set_id": ["663d992d-23cc-4a8e-acd5-a4bea505ba3a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-8869-1)", "package_ndc": "63629-8869-1", "marketing_start_date": "20210930"}], "brand_name": "Solifenacin Succinate", "product_id": "63629-8869_fc62246b-3427-4e5a-9d12-91ecfd2bb342", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "63629-8869", "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": "10 mg/1"}], "application_number": "ANDA210224", "marketing_category": "ANDA", "marketing_start_date": "20190521", "listing_expiration_date": "20261231"}