Package 69842-346-12

Brand: bismuth subsalicylate

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 69842-346-12
Digits Only 6984234612
Product NDC 69842-346
Description

1 BOTTLE in 1 CARTON (69842-346-12) / 24 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-07-06
Brand bismuth subsalicylate
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b96475f-d966-11d4-e063-6394a90a0361", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0050428002391"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["6dd7c01c-5726-e6db-e053-2a91aa0a968d"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-346-12)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-346-12", "marketing_start_date": "20180706"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-346-28)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-346-28", "marketing_start_date": "20180706"}], "brand_name": "Bismuth Subsalicylate", "product_id": "69842-346_4b96475f-d966-11d4-e063-6394a90a0361", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69842-346", "generic_name": "Bismuth Subsalicylate", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bismuth Subsalicylate", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180706", "listing_expiration_date": "20271231"}