Package 63629-8867-1
Brand: solifenacin succinate
Generic: solifenacin succinatePackage Facts
Identity
Package NDC
63629-8867-1
Digits Only
6362988671
Product NDC
63629-8867
Description
30 TABLET, FILM COATED in 1 BOTTLE (63629-8867-1)
Marketing
Marketing Status
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": "0cc29a58-4961-4c78-94cf-330f22b28ba4", "openfda": {"unii": ["KKA5DLD701"], "rxcui": ["477367"], "spl_set_id": ["2dfc5d69-8f35-4f57-90b7-46a5f0f0febe"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-8867-1)", "package_ndc": "63629-8867-1", "marketing_start_date": "20210930"}], "brand_name": "Solifenacin Succinate", "product_id": "63629-8867_0cc29a58-4961-4c78-94cf-330f22b28ba4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "63629-8867", "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"}