cefazolin

Generic: cefazolin sodium

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin sodium
Labeler fresenius kabi usa, llc
Dosage Form POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 500 mg/2.2mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-236
Product ID 63323-236_321ffc80-ee94-4a86-8c33-e966438d9fbb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065303
Listing Expiration 2026-12-31
Marketing Start 2011-07-15

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323236
Hyphenated Format 63323-236

Supplemental Identifiers

RxCUI
1665050 1665052
UPC
0363323237011 0363323236014
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 sodium (source: ndc)
Application Number ANDA065303 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/2.2mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (63323-236-10) / 2.2 mL in 1 VIAL (63323-236-01)
source: ndc

Packages (1)

63323-236-10 25 VIAL in 1 CARTON (63323-236-10) / 2.2 mL in 1 VIAL (63323-236-01)

Ingredients (1)

cefazolin sodium (500 mg/2.2mL)

Linked Drug Pages (1)

CEFAZOLIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "321ffc80-ee94-4a86-8c33-e966438d9fbb", "openfda": {"upc": ["0363323237011", "0363323236014"], "unii": ["P380M0454Z"], "rxcui": ["1665050", "1665052"], "spl_set_id": ["c47c8d14-1eef-40f9-9d11-f0c300b1d4be"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (63323-236-10)  / 2.2 mL in 1 VIAL (63323-236-01)", "package_ndc": "63323-236-10", "marketing_start_date": "20110715"}], "brand_name": "CEFAZOLIN", "product_id": "63323-236_321ffc80-ee94-4a86-8c33-e966438d9fbb", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-236", "generic_name": "CEFAZOLIN SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "500 mg/2.2mL"}], "application_number": "ANDA065303", "marketing_category": "ANDA", "marketing_start_date": "20110715", "listing_expiration_date": "20261231"}