Package 49884-156-76
Brand: varenicline
Generic: varenicline tartratePackage Facts
Identity
Package NDC
49884-156-76
Digits Only
4988415676
Product NDC
49884-156
Description
56 TABLET, FILM COATED in 1 BOTTLE (49884-156-76)
Marketing
Marketing Status
Brand
varenicline
Generic
varenicline tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "98f60ed1-5da2-4d86-a953-111898a5c804", "openfda": {"upc": ["0349884156763", "0349884944995"], "unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["9e5c0ef3-3179-4d7b-bc76-901473c73ce8"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (49884-156-76)", "package_ndc": "49884-156-76", "marketing_start_date": "20210921"}], "brand_name": "Varenicline", "product_id": "49884-156_98f60ed1-5da2-4d86-a953-111898a5c804", "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": "49884-156", "generic_name": "varenicline tartrate", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "active_ingredients": [{"name": "VARENICLINE TARTRATE", "strength": "1 mg/1"}], "application_number": "ANDA201785", "marketing_category": "ANDA", "marketing_start_date": "20210921", "listing_expiration_date": "20261231"}