Package 11673-122-48

Brand: up and up 5-symptom digestive relief

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 11673-122-48
Digits Only 1167312248
Product NDC 11673-122
Description

48 TABLET in 1 BOTTLE, PLASTIC (11673-122-48)

Marketing

Marketing Status
Marketed Since 2019-03-12
Brand up and up 5-symptom 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": "42c2f050-6c70-6c79-e063-6394a90ade8f", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308760"], "spl_set_id": ["7f6b2960-943d-464c-9ff9-4649a8ab4a4e"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 TABLET in 1 BOTTLE, PLASTIC (11673-122-48)", "package_ndc": "11673-122-48", "marketing_start_date": "20190312"}], "brand_name": "up and up 5-symptom digestive relief", "product_id": "11673-122_42c2f050-6c70-6c79-e063-6394a90ade8f", "dosage_form": "TABLET", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "11673-122", "generic_name": "Bismuth subsalicylate", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up 5-symptom digestive relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}