cefazolin
Generic: cefazolin
Labeler: hospira, incDrug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
hospira, inc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 1 g/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04092585
Hyphenated Format
0409-2585
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 25 VIAL in 1 CARTON (0409-2585-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2585-11)
Packages (1)
Ingredients (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"}