Package 51316-171-68

Brand: ultra strength antacid

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 51316-171-68
Digits Only 5131617168
Product NDC 51316-171
Product ID 51316-171_35954e1d-479d-448b-97f3-d9b74c51a9ab
Description

72 TABLET, CHEWABLE in 1 BOTTLE (51316-171-68)

Marketing

Marketing Status
Marketed Since 2025-01-23
Brand ultra strength antacid
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Ultra Strength Antacid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35954e1d-479d-448b-97f3-d9b74c51a9ab", "openfda": {"upc": ["0050428380710"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["2bc4c71c-a9c5-17df-e063-6294a90ac88c"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (51316-171-68)", "package_ndc": "51316-171-68", "marketing_start_date": "20250123"}], "brand_name": "Ultra Strength Antacid", "product_id": "51316-171_35954e1d-479d-448b-97f3-d9b74c51a9ab", "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": "51316-171", "generic_name": "Calcium carbonate", "labeler_name": "CVS", "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": "20250123", "listing_expiration_date": "20261231"}