Package 53041-126-17

Brand: alkums antacid

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 53041-126-17
Digits Only 5304112617
Product NDC 53041-126
Description

150 TABLET, CHEWABLE in 1 BOTTLE (53041-126-17)

Marketing

Marketing Status
Marketed Since 2012-02-01
Brand alkums antacid
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8834ce9-ce9f-4e00-abf4-d9a1f6e7e84d", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["210111", "308907"], "spl_set_id": ["7451cd9f-1723-46d0-837e-8dc48bfb6bba"], "manufacturer_name": ["Guardian Drug Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, CHEWABLE in 1 BOTTLE (53041-126-17)", "package_ndc": "53041-126-17", "marketing_start_date": "20120201"}], "brand_name": "Alkums antacid", "product_id": "53041-126_f8834ce9-ce9f-4e00-abf4-d9a1f6e7e84d", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "53041-126", "generic_name": "calcium carbonate", "labeler_name": "Guardian Drug Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alkums antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120201", "listing_expiration_date": "20261231"}