Package 51316-908-75

Brand: ultra strength antacid

Generic: calcium carbonate chewable tablets
NDC Package

Package Facts

Identity

Package NDC 51316-908-75
Digits Only 5131690875
Product NDC 51316-908
Description

72 TABLET, CHEWABLE in 1 BOTTLE (51316-908-75)

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand ultra strength antacid
Generic calcium carbonate chewable tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b59ddbc-d30c-355d-e063-6394a90a7b84", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["24cec2bc-cf12-b513-e063-6394a90a9447"], "manufacturer_name": ["CVS Pharmacy. Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (51316-908-75)", "package_ndc": "51316-908-75", "marketing_start_date": "20250401"}], "brand_name": "Ultra Strength Antacid", "product_id": "51316-908_2b59ddbc-d30c-355d-e063-6394a90a7b84", "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": "51316-908", "generic_name": "Calcium Carbonate Chewable Tablets", "labeler_name": "CVS Pharmacy. Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}