Package 21130-125-40

Brand: digestive relief

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 21130-125-40
Digits Only 2113012540
Product NDC 21130-125
Description

1 BOTTLE in 1 CARTON (21130-125-40) / 40 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-10-05
Brand digestive relief
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "424aa911-6748-010b-e063-6394a90a7ae7", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["5538d56a-b258-4260-b51b-f5131bd76885"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["SAFEWAY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-125-40)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-125-40", "marketing_start_date": "20201005"}], "brand_name": "Digestive Relief", "product_id": "21130-125_424aa911-6748-010b-e063-6394a90a7ae7", "dosage_form": "TABLET, FILM COATED", "product_ndc": "21130-125", "generic_name": "Bismuth Subsalicylate", "labeler_name": "SAFEWAY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Digestive Relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201005", "listing_expiration_date": "20261231"}