Package 0135-0098-26

Brand: gaviscon extra strength

Generic: aluminum hydroxide and magnesium carbonate
NDC Package

Package Facts

Identity

Package NDC 0135-0098-26
Digits Only 0135009826
Product NDC 0135-0098
Product ID 0135-0098_02f611d3-df31-4514-86ae-9e81004acdbf
Description

100 TABLET, CHEWABLE in 1 BOTTLE (0135-0098-26)

Marketing

Marketing Status
Marketed Since 2011-06-13
Brand gaviscon extra strength
Generic aluminum hydroxide and magnesium carbonate
Sample Package No

Linked Drug Pages (1)

Gaviscon Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "02f611d3-df31-4514-86ae-9e81004acdbf", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["212978", "308072"], "spl_set_id": ["7f367927-c366-465c-a059-e2cfb337d562"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (0135-0098-26)", "package_ndc": "0135-0098-26", "marketing_start_date": "20110613"}], "brand_name": "Gaviscon Extra Strength", "product_id": "0135-0098_02f611d3-df31-4514-86ae-9e81004acdbf", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0135-0098", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gaviscon", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "160 mg/1"}, {"name": "MAGNESIUM CARBONATE", "strength": "105 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110613", "listing_expiration_date": "20261231"}