cefazolin

Generic: cefazolin

Labeler: hospira, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler hospira, inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cefazolin sodium 1 g/1

Manufacturer
Hospira, Inc

Identifiers & Regulatory

Product NDC 0409-2585
Product ID 0409-2585_2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065345
Marketing Start 2007-05-09
Marketing End 2026-09-30

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04092585
Hyphenated Format 0409-2585

Supplemental Identifiers

RxCUI
1665050
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 ANDA065345 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (0409-2585-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2585-11)
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (1 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["62441488-fc97-4535-a249-4485fb075022"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0409-2585-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2585-11)", "package_ndc": "0409-2585-01", "marketing_end_date": "20260930", "marketing_start_date": "20070807"}], "brand_name": "Cefazolin", "product_id": "0409-2585_2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0409-2585", "generic_name": "Cefazolin", "labeler_name": "Hospira, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065345", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20070509"}