Package 0135-0553-01

Brand: tums ultra

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 0135-0553-01
Digits Only 0135055301
Product NDC 0135-0553
Product ID 0135-0553_80b36d79-a112-426a-ae40-5c4371258157
Description

72 TABLET, CHEWABLE in 1 BOTTLE (0135-0553-01)

Marketing

Marketing Status
Marketed Since 2023-03-01
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": "80b36d79-a112-426a-ae40-5c4371258157", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892", "1044524"], "spl_set_id": ["c544120f-15f0-48b5-88b2-d4820f180f50"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (0135-0553-01)", "package_ndc": "0135-0553-01", "marketing_start_date": "20230301"}], "brand_name": "Tums Ultra", "product_id": "0135-0553_80b36d79-a112-426a-ae40-5c4371258157", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0135-0553", "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": "20230301", "listing_expiration_date": "20261231"}