Package 63868-565-12

Brand: heartburn relief

Generic: aluminum hydroxide and magnesium carbonate
NDC Package

Package Facts

Identity

Package NDC 63868-565-12
Digits Only 6386856512
Product NDC 63868-565
Description

355 mL in 1 BOTTLE (63868-565-12)

Marketing

Marketing Status
Marketed Since 2019-11-01
Brand heartburn relief
Generic aluminum hydroxide and magnesium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "097f7264-6848-61fb-e063-6294a90a3f2f", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["245001"], "spl_set_id": ["b4656a2f-a866-5f7a-e053-2995a90ac2c2"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (63868-565-12)", "package_ndc": "63868-565-12", "marketing_start_date": "20191101"}], "brand_name": "HEARTBURN RELIEF", "product_id": "63868-565_097f7264-6848-61fb-e063-6294a90a3f2f", "dosage_form": "SUSPENSION", "product_ndc": "63868-565", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HEARTBURN RELIEF", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "254 mg/5mL"}, {"name": "MAGNESIUM CARBONATE", "strength": "237.5 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}