Package 0135-0246-04
Brand: tums smoothies
Generic: calcium carbonatePackage Facts
Identity
Package NDC
0135-0246-04
Digits Only
0135024604
Product NDC
0135-0246
Description
72 TABLET, CHEWABLE in 1 BOTTLE (0135-0246-04)
Marketing
Marketing Status
Brand
tums smoothies
Generic
calcium carbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2935b6b2-d48d-49d7-b4db-d0d4c9aa34d1", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308915", "1044532"], "spl_set_id": ["c22944b8-8733-4689-be0c-f320467f79ea"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, CHEWABLE in 1 CELLO PACK (0135-0246-01)", "package_ndc": "0135-0246-01", "marketing_start_date": "20100324"}, {"sample": false, "description": "60 TABLET, CHEWABLE in 1 BOTTLE (0135-0246-02)", "package_ndc": "0135-0246-02", "marketing_start_date": "20100324"}, {"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (0135-0246-04)", "package_ndc": "0135-0246-04", "marketing_start_date": "20170314"}, {"sample": false, "description": "140 TABLET, CHEWABLE in 1 BOTTLE (0135-0246-05)", "package_ndc": "0135-0246-05", "marketing_start_date": "20140810"}, {"sample": false, "description": "250 TABLET, CHEWABLE in 1 BOTTLE (0135-0246-07)", "package_ndc": "0135-0246-07", "marketing_start_date": "20160126"}], "brand_name": "TUMS Smoothies", "product_id": "0135-0246_2935b6b2-d48d-49d7-b4db-d0d4c9aa34d1", "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": "0135-0246", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUMS", "brand_name_suffix": "Smoothies", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "750 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100324", "listing_expiration_date": "20261231"}