Package 50090-7135-0

Brand: varenicline

Generic: varenicline tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7135-0
Digits Only 5009071350
Product NDC 50090-7135
Product ID 50090-7135_cc56f26e-8b25-442c-a8b1-c3dfc7fee841
Description

56 TABLET, FILM COATED in 1 BOTTLE (50090-7135-0)

Marketing

Marketing Status
Marketed Since 2024-04-19
Brand varenicline
Generic varenicline tartrate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc56f26e-8b25-442c-a8b1-c3dfc7fee841", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671"], "spl_set_id": ["2d5dfa6e-e69d-414a-8ff2-44714debbbe2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (50090-7135-0)", "package_ndc": "50090-7135-0", "marketing_start_date": "20240419"}], "brand_name": "varenicline", "product_id": "50090-7135_cc56f26e-8b25-442c-a8b1-c3dfc7fee841", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]", "Partial Cholinergic Nicotinic Agonist [EPC]", "Partial Cholinergic Nicotinic Agonists [MoA]"], "product_ndc": "50090-7135", "generic_name": "varenicline tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": ".5 mg/1"}], "application_number": "ANDA214557", "marketing_category": "ANDA", "marketing_start_date": "20230825", "listing_expiration_date": "20261231"}