Package 71921-307-51

Brand: varenicline

Generic: varenicline tartrate
NDC Package

Package Facts

Identity

Package NDC 71921-307-51
Digits Only 7192130751
Product NDC 71921-307
Product ID 71921-307_2b9c8b1e-6193-4d8e-9b50-6aca27294263
Description

1 KIT in 1 CARTON (71921-307-51) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-11-01
Brand varenicline
Generic varenicline tartrate
Sample Package No

Linked Drug Pages (1)

Varenicline, Varenicline tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "2b9c8b1e-6193-4d8e-9b50-6aca27294263", "openfda": {"unii": ["82269ASB48"], "rxcui": ["636671", "636676", "749289"], "spl_set_id": ["2b9c8b1e-6193-4d8e-9b50-6aca27294263"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (71921-307-51)  *  11 TABLET, FILM COATED in 1 BLISTER PACK *  42 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71921-307-51", "marketing_start_date": "20241101"}], "brand_name": "Varenicline", "product_id": "71921-307_2b9c8b1e-6193-4d8e-9b50-6aca27294263", "dosage_form": "KIT", "product_ndc": "71921-307", "generic_name": "Varenicline Tartrate", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Varenicline", "application_number": "ANDA219106", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}