tums ex

Generic: calcium carbonate

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tums ex
Generic Name calcium carbonate
Labeler haleon us holdings llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

calcium carbonate 750 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0178
Product ID 0135-0178_3ce3175f-47e7-4ea3-b5b6-836368fc7522
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2010-01-18

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350178
Hyphenated Format 0135-0178

Supplemental Identifiers

RxCUI
308915 1044532
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tums ex (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 48 TABLET in 1 BOTTLE (0135-0178-02)
  • 96 TABLET in 1 BOTTLE (0135-0178-03)
  • 70 TABLET in 1 BOTTLE (0135-0178-05)
  • 8 TABLET in 1 PACKAGE (0135-0178-08)
  • 200 TABLET in 1 BOTTLE (0135-0178-09)
source: ndc

Packages (5)

0135-0178-02 48 TABLET in 1 BOTTLE (0135-0178-02) 0135-0178-03 96 TABLET in 1 BOTTLE (0135-0178-03) 0135-0178-05 70 TABLET in 1 BOTTLE (0135-0178-05) 0135-0178-08 8 TABLET in 1 PACKAGE (0135-0178-08) 0135-0178-09 200 TABLET in 1 BOTTLE (0135-0178-09)

Ingredients (1)

calcium carbonate (750 mg/1)

Linked Drug Pages (1)

TUMS EX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ce3175f-47e7-4ea3-b5b6-836368fc7522", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308915", "1044532"], "spl_set_id": ["593a0494-d669-4bcf-8412-b92645b2d76c"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 TABLET in 1 BOTTLE (0135-0178-02)", "package_ndc": "0135-0178-02", "marketing_start_date": "20100118"}, {"sample": false, "description": "96 TABLET in 1 BOTTLE (0135-0178-03)", "package_ndc": "0135-0178-03", "marketing_start_date": "20100118"}, {"sample": false, "description": "70 TABLET in 1 BOTTLE (0135-0178-05)", "package_ndc": "0135-0178-05", "marketing_start_date": "20100118"}, {"sample": false, "description": "8 TABLET in 1 PACKAGE (0135-0178-08)", "package_ndc": "0135-0178-08", "marketing_start_date": "20100118"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (0135-0178-09)", "package_ndc": "0135-0178-09", "marketing_start_date": "20100118"}], "brand_name": "TUMS EX", "product_id": "0135-0178_3ce3175f-47e7-4ea3-b5b6-836368fc7522", "dosage_form": "TABLET", "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": "0135-0178", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUMS", "brand_name_suffix": "EX", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "750 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100118", "listing_expiration_date": "20261231"}