Package 0322-2222-04

Brand: percy medicine

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 0322-2222-04
Digits Only 0322222204
Product NDC 0322-2222
Description

118 mL in 1 BOTTLE (0322-2222-04)

Marketing

Marketing Status
Marketed Since 2019-09-09
Brand percy medicine
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "920b3bd5-7ef1-43b7-a7ce-015b880f4b41", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["616343", "1233767"], "spl_set_id": ["08dd53b7-8345-4849-9155-60429cbe2c51"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Merrick Medicine Company, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (0322-2222-04)", "package_ndc": "0322-2222-04", "marketing_start_date": "20190909"}], "brand_name": "Percy Medicine", "product_id": "0322-2222_920b3bd5-7ef1-43b7-a7ce-015b880f4b41", "dosage_form": "LIQUID", "product_ndc": "0322-2222", "generic_name": "Bismuth Subsalicylate", "labeler_name": "Merrick Medicine Company, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Percy Medicine", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "1050 mg/10mL"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190909", "listing_expiration_date": "20261231"}