Package 30142-138-24

Brand: ultra strength digestive relief

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 30142-138-24
Digits Only 3014213824
Product NDC 30142-138
Description

1 BOTTLE in 1 CARTON (30142-138-24) / 24 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-11-18
Brand ultra strength 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": "3b873634-dbad-e0bc-e063-6294a90a5f74", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0041260008542"], "unii": ["62TEY51RR1"], "rxcui": ["1998447"], "spl_set_id": ["5e288108-1578-4379-a3d6-44b447187643"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["THE KROGER CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-138-24)  / 24 TABLET in 1 BOTTLE", "package_ndc": "30142-138-24", "marketing_start_date": "20191118"}], "brand_name": "Ultra Strength digestive relief", "product_id": "30142-138_3b873634-dbad-e0bc-e063-6294a90a5f74", "dosage_form": "TABLET", "product_ndc": "30142-138", "generic_name": "Bismuth subsalicylate", "labeler_name": "THE KROGER CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength digestive relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191118", "listing_expiration_date": "20261231"}