Package 0135-0094-41

Brand: gaviscon

Generic: aluminum hydroxide and magnesium carbonate
NDC Package

Package Facts

Identity

Package NDC 0135-0094-41
Digits Only 0135009441
Product NDC 0135-0094
Product ID 0135-0094_4aba2043-4dde-0c18-e063-6294a90a5fcf
Description

355 mL in 1 BOTTLE (0135-0094-41)

Marketing

Marketing Status
Marketed Since 2011-01-14
Brand gaviscon
Generic aluminum hydroxide and magnesium carbonate
Sample Package No

Linked Drug Pages (1)

GAVISCON ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4aba2043-4dde-0c18-e063-6294a90a5fcf", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["245001", "252203", "404472", "1251365"], "spl_set_id": ["2d74e5bc-1f10-4fb6-9258-cd906e360013"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (0135-0094-41)", "package_ndc": "0135-0094-41", "marketing_start_date": "20110114"}, {"sample": false, "description": "177 mL in 1 BOTTLE (0135-0094-42)", "package_ndc": "0135-0094-42", "marketing_start_date": "20110114"}], "brand_name": "GAVISCON", "product_id": "0135-0094_4aba2043-4dde-0c18-e063-6294a90a5fcf", "dosage_form": "LIQUID", "product_ndc": "0135-0094", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GAVISCON", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "95 mg/15mL"}, {"name": "MAGNESIUM CARBONATE", "strength": "358 mg/15mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110114", "listing_expiration_date": "20271231"}