Package 17714-041-01

Brand: antacid

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 17714-041-01
Digits Only 1771404101
Product NDC 17714-041
Description

100 TABLET, CHEWABLE in 1 BOTTLE (17714-041-01)

Marketing

Marketing Status
Marketed Since 2007-11-30
Brand antacid
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a327df7-e74f-8130-e063-6294a90a6e83", "openfda": {"upc": ["0017714041014"], "unii": ["H0G9379FGK"], "rxcui": ["308907"], "spl_set_id": ["3203dfc5-2cb1-4703-8d81-63fba07ddd98"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (17714-041-01)", "package_ndc": "17714-041-01", "marketing_start_date": "20071130"}], "brand_name": "ANTACID", "product_id": "17714-041_2a327df7-e74f-8130-e063-6294a90a6e83", "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": "17714-041", "generic_name": "Calcium Carbonate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20071130", "listing_expiration_date": "20261231"}