Package 0135-0235-01

Brand: tums ultra

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 0135-0235-01
Digits Only 0135023501
Product NDC 0135-0235
Product ID 0135-0235_89045f58-6d59-4843-86d3-ebe5450390f9
Description

72 TABLET, CHEWABLE in 1 BOTTLE (0135-0235-01)

Marketing

Marketing Status
Marketed Since 2021-06-21
Brand tums ultra
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

TUMS ULTRA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "89045f58-6d59-4843-86d3-ebe5450390f9", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892", "1044524"], "spl_set_id": ["348d3dfa-6a52-4583-96e3-83c4bf2df45b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (0135-0235-01)", "package_ndc": "0135-0235-01", "marketing_start_date": "20210621"}, {"sample": false, "description": "160 TABLET, CHEWABLE in 1 BOTTLE (0135-0235-02)", "package_ndc": "0135-0235-02", "marketing_start_date": "20210723"}], "brand_name": "TUMS ULTRA", "product_id": "0135-0235_89045f58-6d59-4843-86d3-ebe5450390f9", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0135-0235", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUMS", "brand_name_suffix": "ULTRA", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210621", "listing_expiration_date": "20261231"}