Package 68788-8239-3

Brand: major bismuth subsalicylate

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 68788-8239-3
Digits Only 6878882393
Product NDC 68788-8239
Description

5 BLISTER PACK in 1 BOX (68788-8239-3) / 6 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-02-07
Brand major 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": "522d86cb-c655-43c1-b704-0c12a9a220d7", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308761"], "spl_set_id": ["69b9999f-c2e5-43a6-891f-0e24d3c343a4"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 BOX (68788-8239-3)  / 6 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "68788-8239-3", "marketing_start_date": "20250207"}], "brand_name": "Major Bismuth Subsalicylate", "product_id": "68788-8239_522d86cb-c655-43c1-b704-0c12a9a220d7", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "68788-8239", "generic_name": "Bismuth subsalicylate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Major Bismuth Subsalicylate", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211011", "listing_expiration_date": "20261231"}