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
INTRAVENOUS
Active Ingredients

cefazolin sodium 10 g/1

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-238
Product ID 63323-238_9684b8e0-7438-41d9-89e1-b217b5568360
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065306
Listing Expiration 2026-12-31
Marketing Start 2011-06-14

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323238
Hyphenated Format 63323-238

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 sodium (source: ndc)
Application Number ANDA065306 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (63323-238-61) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-238-01)
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (10 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9684b8e0-7438-41d9-89e1-b217b5568360", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["313920"], "spl_set_id": ["47a8928f-708d-418a-829b-36eded96bac0"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-238-61)  / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-238-01)", "package_ndc": "63323-238-61", "marketing_start_date": "20110614"}], "brand_name": "Cefazolin", "product_id": "63323-238_9684b8e0-7438-41d9-89e1-b217b5568360", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-238", "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": "10 g/1"}], "application_number": "ANDA065306", "marketing_category": "ANDA", "marketing_start_date": "20110614", "listing_expiration_date": "20261231"}