Package 11673-933-72

Brand: ultra strength antacid

Generic: antacid
NDC Package

Package Facts

Identity

Package NDC 11673-933-72
Digits Only 1167393372
Product NDC 11673-933
Product ID 11673-933_42c23ba3-b826-b876-e063-6394a90a1795
Description

72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-933-72)

Marketing

Marketing Status
Marketed Since 2018-01-05
Brand ultra strength antacid
Generic antacid
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": "42c23ba3-b826-b876-e063-6394a90a1795", "openfda": {"upc": ["0492450504199"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["2125e81b-23c6-4c5f-a6aa-829f8d3df71f"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-933-72)", "package_ndc": "11673-933-72", "marketing_start_date": "20180105"}], "brand_name": "ultra strength antacid", "product_id": "11673-933_42c23ba3-b826-b876-e063-6394a90a1795", "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": "11673-933", "generic_name": "Antacid", "labeler_name": "Target Corporation", "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": "20180105", "listing_expiration_date": "20261231"}