Package 0363-1302-02

Brand: ultra strength digestive relief

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 0363-1302-02
Digits Only 0363130202
Product NDC 0363-1302
Product ID 0363-1302_447d20f5-798d-ca2a-e063-6294a90ada0d
Description

1 BOTTLE in 1 CARTON (0363-1302-02) / 24 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-09-26
Brand ultra strength digestive relief
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Ultra Strength digestive relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "447d20f5-798d-ca2a-e063-6294a90ada0d", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["1998447"], "spl_set_id": ["756e7a47-7e14-4694-84fa-ca6396f7edcc"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1302-02)  / 24 TABLET in 1 BOTTLE", "package_ndc": "0363-1302-02", "marketing_start_date": "20220926"}], "brand_name": "Ultra Strength digestive relief", "product_id": "0363-1302_447d20f5-798d-ca2a-e063-6294a90ada0d", "dosage_form": "TABLET", "product_ndc": "0363-1302", "generic_name": "Bismuth subsalicylate", "labeler_name": "WALGREENS 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": "20220926", "listing_expiration_date": "20261231"}