Package 49580-0842-8

Brand: stomach relief ultra strength

Generic: bismuth subsalicylate
NDC Package

Package Facts

Identity

Package NDC 49580-0842-8
Digits Only 4958008428
Product NDC 49580-0842
Description

237 mL in 1 BOTTLE, PLASTIC (49580-0842-8)

Marketing

Marketing Status
Marketed Since 2019-02-28
Brand stomach relief ultra strength
Generic bismuth subsalicylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2098abda-1027-4fc4-b273-2a0f39316a41", "openfda": {"nui": ["M0002611", "N0000180183"], "upc": ["0349580842090"], "unii": ["62TEY51RR1"], "rxcui": ["308763"], "spl_set_id": ["cb5ca7ab-39cf-4b07-ac22-a00b214db102"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (49580-0842-8)", "package_ndc": "49580-0842-8", "marketing_start_date": "20190228"}], "brand_name": "Stomach Relief Ultra Strength", "product_id": "49580-0842_2098abda-1027-4fc4-b273-2a0f39316a41", "dosage_form": "LIQUID", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "49580-0842", "generic_name": "Bismuth subsalicylate", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stomach Relief", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "525 mg/15mL"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}