cefazolin

Generic: cefazolin

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefazolin sodium 3 g/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9140
Product ID 0143-9140_e32063de-96fe-4fb4-9176-5a9d6dc4a722
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA216109
Listing Expiration 2026-12-31
Marketing Start 2023-03-01

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439140
Hyphenated Format 0143-9140

Supplemental Identifiers

RxCUI
1665060 2630753
UNII
P380M0454Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefazolin (source: ndc)
Generic Name cefazolin (source: ndc)
Application Number NDA216109 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (0143-9140-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (3 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e32063de-96fe-4fb4-9176-5a9d6dc4a722", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665060", "2630753"], "spl_set_id": ["6c7761d3-c154-4802-9876-627cd42913f0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9140-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9140-25", "marketing_start_date": "20230301"}], "brand_name": "Cefazolin", "product_id": "0143-9140_e32063de-96fe-4fb4-9176-5a9d6dc4a722", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9140", "generic_name": "Cefazolin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "3 g/1"}], "application_number": "NDA216109", "marketing_category": "NDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}