Package 17856-3117-3

Brand: calcium carbonate

Generic: calcium carbonate
NDC Package

Package Facts

Identity

Package NDC 17856-3117-3
Digits Only 1785631173
Product NDC 17856-3117
Description

5 mL in 1 CUP (17856-3117-3)

Marketing

Marketing Status
Marketed Since 2021-01-28
Brand calcium carbonate
Generic calcium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34f3682a-e5bc-851a-e063-6394a90a8e96", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308891"], "spl_set_id": ["38654d22-2f8a-49d2-a1cd-06d341f11323"], "manufacturer_name": ["Atlantic Biologicals Corps"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 CUP (17856-3117-3)", "package_ndc": "17856-3117-3", "marketing_start_date": "20210128"}], "brand_name": "Calcium Carbonate", "product_id": "17856-3117_34f3682a-e5bc-851a-e063-6394a90a8e96", "dosage_form": "SUSPENSION", "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": "17856-3117", "generic_name": "Calcium Carbonate", "labeler_name": "Atlantic Biologicals Corps", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Calcium Carbonate", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1250 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20041201", "listing_expiration_date": "20261231"}