Package 51662-1347-1

Brand: calcium gluconate

Generic: calcium gluconate
NDC Package

Package Facts

Identity

Package NDC 51662-1347-1
Digits Only 5166213471
Product NDC 51662-1347
Description

50 mL in 1 VIAL, PLASTIC (51662-1347-1)

Marketing

Marketing Status
Marketed Since 2018-12-21
Brand calcium gluconate
Generic calcium gluconate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef7bd5a0-02a5-7b66-e053-2995a90a8ffa", "openfda": {"unii": ["CZN0MI5R31"], "rxcui": ["1668248"], "spl_set_id": ["7d93251a-b555-0be0-e053-2991aa0ad764"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, PLASTIC (51662-1347-1)", "package_ndc": "51662-1347-1", "marketing_start_date": "20181221"}], "brand_name": "CALCIUM GLUCONATE", "product_id": "51662-1347_ef7bd5a0-02a5-7b66-e053-2995a90a8ffa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]"], "product_ndc": "51662-1347", "generic_name": "CALCIUM GLUCONATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CALCIUM GLUCONATE", "active_ingredients": [{"name": "CALCIUM GLUCONATE MONOHYDRATE", "strength": "98 mg/mL"}], "application_number": "NDA208418", "marketing_category": "NDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}