Package 70000-0683-1

Brand: antacid ultra strength

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 70000-0683-1
Digits Only 7000006831
Product NDC 70000-0683
Product ID 70000-0683_411d7abc-9cd4-0480-e063-6394a90a8bb8
Description

72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1)

Marketing

Marketing Status
Marketed Since 2024-07-08
Brand antacid ultra strength
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

ANTACID Ultra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "411d7abc-9cd4-0480-e063-6394a90a8bb8", "openfda": {"upc": ["0096295143577"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["d267ca31-09bd-46d3-be08-a259642f1b7f"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1)", "package_ndc": "70000-0683-1", "marketing_start_date": "20240708"}], "brand_name": "ANTACID Ultra Strength", "product_id": "70000-0683_411d7abc-9cd4-0480-e063-6394a90a8bb8", "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": "70000-0683", "generic_name": "calcium carbonate", "labeler_name": "CARDINAL HEALTH 110, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240708", "listing_expiration_date": "20261231"}