cefazolin
Generic: cefazolin
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 3 g/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439140
Hyphenated Format
0143-9140
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
NDA216109 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 g/1
Packaging
- 25 VIAL in 1 CARTON (0143-9140-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (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"}