Package 70518-4299-0

Brand: calcium acetate

Generic: calcium acetate
NDC Package

Package Facts

Identity

Package NDC 70518-4299-0
Digits Only 7051842990
Product NDC 70518-4299
Description

30 CAPSULE in 1 BLISTER PACK (70518-4299-0)

Marketing

Marketing Status
Marketed Since 2025-03-02
Brand calcium acetate
Generic calcium acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "402d6654-d9f1-7c95-e063-6394a90a6587", "openfda": {"unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["89a2ee04-1024-4a81-ba0d-a6655d529827"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4299-0)", "package_ndc": "70518-4299-0", "marketing_start_date": "20250302"}], "brand_name": "calcium acetate", "product_id": "70518-4299_402d6654-d9f1-7c95-e063-6394a90a6587", "dosage_form": "CAPSULE", "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": "70518-4299", "generic_name": "calcium acetate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "calcium acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA202315", "marketing_category": "ANDA", "marketing_start_date": "20250302", "listing_expiration_date": "20261231"}