Package 70000-0594-1

Brand: bismuth subsalicylate

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 70000-0594-1
Digits Only 7000005941
Product NDC 70000-0594
Product ID 70000-0594_2de450b8-01e2-0e3b-e063-6394a90af5f7
Description

1 BOTTLE in 1 CARTON (70000-0594-1) / 24 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-01-03
Brand bismuth subsalicylate
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Bismuth Subsalicylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2de450b8-01e2-0e3b-e063-6394a90af5f7", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0096295141375"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["d4af6694-910c-da17-e053-2995a90a8454"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["LEADER/ Cardinal Health 110, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70000-0594-1)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "70000-0594-1", "marketing_start_date": "20220103"}], "brand_name": "Bismuth Subsalicylate", "product_id": "70000-0594_2de450b8-01e2-0e3b-e063-6394a90af5f7", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70000-0594", "generic_name": "Bismuth Subsalicylate", "labeler_name": "LEADER/ Cardinal Health 110, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bismuth Subsalicylate", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220103", "listing_expiration_date": "20261231"}