Package 17714-045-30

Brand: pepto relief

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 17714-045-30
Digits Only 1771404530
Product NDC 17714-045
Description

30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30)

Marketing

Marketing Status
Marketed Since 2002-01-09
Brand pepto 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": "60f4322f-5cb1-096a-e053-2a91aa0a64eb", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0017714045302"], "unii": ["62TEY51RR1"], "rxcui": ["308761"], "spl_set_id": ["a02babe7-9255-44c7-90e1-b5ad5e59c72a"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (17714-045-30)", "package_ndc": "17714-045-30", "marketing_start_date": "20020109"}], "brand_name": "Pepto Relief", "product_id": "17714-045_60f4322f-5cb1-096a-e053-2a91aa0a64eb", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "17714-045", "generic_name": "Bismuth subsalicylate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pepto Relief", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "part335", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20020109", "listing_expiration_date": "20261231"}