cefazolin

Generic: cefazolin

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA 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 20 g/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9665
Product ID 0143-9665_a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065143
Listing Expiration 2026-12-31
Marketing Start 2004-10-18

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439665
Hyphenated Format 0143-9665

Supplemental Identifiers

RxCUI
313920
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 ANDA065143 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 g/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)
source: ndc

Packages (1)

0143-9665-10 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)

Ingredients (1)

cefazolin sodium (20 g/1)

Linked Drug Pages (1)

Cefazolin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["313920"], "spl_set_id": ["06091653-e568-4e82-acc7-aefbce16de17"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)", "package_ndc": "0143-9665-10", "marketing_start_date": "20041018"}], "brand_name": "Cefazolin", "product_id": "0143-9665_a1fc6bdd-6f1b-402f-9e84-b6e5ed5febb4", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9665", "generic_name": "Cefazolin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "20 g/1"}], "application_number": "ANDA065143", "marketing_category": "ANDA", "marketing_start_date": "20041018", "listing_expiration_date": "20261231"}