Package 0135-0611-01

Brand: tums regular strength

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 0135-0611-01
Digits Only 0135061101
Product NDC 0135-0611
Description

150 TABLET, CHEWABLE in 1 BOTTLE (0135-0611-01)

Marketing

Marketing Status
Marketed Since 2016-09-01
Brand tums regular strength
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "12c98e11-49eb-b55e-e063-6394a90ae122", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["210117", "308907"], "spl_set_id": ["ac80f627-3f51-425b-8c75-e07363048b00"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, CHEWABLE in 1 BOTTLE (0135-0611-01)", "package_ndc": "0135-0611-01", "marketing_start_date": "20160901"}], "brand_name": "Tums Regular Strength", "product_id": "0135-0611_12c98e11-49eb-b55e-e063-6394a90ae122", "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": "0135-0611", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tums", "brand_name_suffix": "Regular Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160901", "listing_expiration_date": "20261231"}