Package 60505-4702-3

Brand: solifenacin succinate

Generic: solifenacin succinate
NDC Package

Package Facts

Identity

Package NDC 60505-4702-3
Digits Only 6050547023
Product NDC 60505-4702
Description

30 TABLET, FILM COATED in 1 BOTTLE (60505-4702-3)

Marketing

Marketing Status
Discontinued 2027-11-30
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": "70d28c29-7862-4ead-a53f-d3646aba26dd", "openfda": {"upc": ["0360505470235", "0360505470334"], "unii": ["KKA5DLD701"], "rxcui": ["477367", "477372"], "spl_set_id": ["1d96b386-febf-a510-a896-033e832c8f30"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-4702-3)", "package_ndc": "60505-4702-3", "marketing_end_date": "20271130", "marketing_start_date": "20190520"}], "brand_name": "Solifenacin Succinate", "product_id": "60505-4702_70d28c29-7862-4ead-a53f-d3646aba26dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "60505-4702", "generic_name": "Solifenacin Succinate", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solifenacin Succinate", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "5 mg/1"}], "application_number": "ANDA209333", "marketing_category": "ANDA", "marketing_end_date": "20271130", "marketing_start_date": "20190520"}