Package 17714-025-10

Brand: antacid

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 17714-025-10
Digits Only 1771402510
Product NDC 17714-025
Product ID 17714-025_60f41580-e08d-faad-e053-2a91aa0a9076
Description

1000 TABLET in 1 BOTTLE (17714-025-10)

Marketing

Marketing Status
Marketed Since 1990-04-06
Brand antacid
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

ANTACID ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e08d-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714025014"], "unii": ["H0G9379FGK"], "rxcui": ["577040"], "spl_set_id": ["0108b97f-02e9-4f86-9f33-cde4f919affd"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-025-01)", "package_ndc": "17714-025-01", "marketing_start_date": "19900406"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-025-10)", "package_ndc": "17714-025-10", "marketing_start_date": "19900406"}], "brand_name": "ANTACID", "product_id": "17714-025_60f41580-e08d-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]"], "product_ndc": "17714-025", "generic_name": "Calcium Carbonate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "648 mg/1"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "19900406", "listing_expiration_date": "20261231"}