Package 70771-1774-6
Brand: varenicline
Generic: vareniclinePackage Facts
Identity
Package NDC
70771-1774-6
Digits Only
7077117746
Product NDC
70771-1774
Description
56 TABLET, FILM COATED in 1 BOTTLE (70771-1774-6)
Marketing
Marketing Status
Brand
varenicline
Generic
varenicline
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "df89bfa8-f749-4840-a207-6499b82516f5", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676"], "spl_set_id": ["481b94af-ee34-44be-8ca1-b2415525efac"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (70771-1774-6)", "package_ndc": "70771-1774-6", "marketing_start_date": "20230613"}], "brand_name": "Varenicline", "product_id": "70771-1774_df89bfa8-f749-4840-a207-6499b82516f5", "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": "70771-1774", "generic_name": "Varenicline", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA216723", "marketing_category": "ANDA", "marketing_start_date": "20230613", "listing_expiration_date": "20261231"}