Package 67184-1001-2

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 67184-1001-2
Digits Only 6718410012
Product NDC 67184-1001
Description

25 VIAL in 1 CARTON (67184-1001-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2015-12-28
Brand cefazolin
Generic cefazolin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0cc53b72-80e0-4a82-e063-6394a90a7fdf", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665060"], "spl_set_id": ["e8bd9e95-8af5-416b-b58c-e1dbe3d052ac"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (67184-1001-2)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "67184-1001-2", "marketing_start_date": "20151228"}], "brand_name": "Cefazolin", "product_id": "67184-1001_0cc53b72-80e0-4a82-e063-6394a90a7fdf", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1001", "generic_name": "Cefazolin", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20151228", "listing_expiration_date": "20261231"}