cefazolin

Generic: cefazolin

Labeler: henry schein inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler henry schein inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 225 mg/mL

Manufacturer
Henry Schein Inc.

Identifiers & Regulatory

Product NDC 0404-9835
Product ID 0404-9835_a5e569a1-da41-44da-a31a-3c9d2c0b61c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065047
Listing Expiration 2026-12-31
Marketing Start 2022-01-09

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049835
Hyphenated Format 0404-9835

Supplemental Identifiers

RxCUI
1665052
UNII
P380M0454Z

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 ANDA065047 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 225 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9835-99) / 2.2 mL in 1 VIAL
source: ndc

Packages (1)

0404-9835-99 1 VIAL in 1 BAG (0404-9835-99) / 2.2 mL in 1 VIAL

Ingredients (1)

cefazolin sodium (225 mg/mL)

Linked Drug Pages (1)

CEFAZOLIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a5e569a1-da41-44da-a31a-3c9d2c0b61c2", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665052"], "spl_set_id": ["922fb1a1-ad4c-4a12-8d5d-00fe13af18e8"], "manufacturer_name": ["Henry Schein Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9835-99)  / 2.2 mL in 1 VIAL", "package_ndc": "0404-9835-99", "marketing_start_date": "20220109"}], "brand_name": "CEFAZOLIN", "product_id": "0404-9835_a5e569a1-da41-44da-a31a-3c9d2c0b61c2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0404-9835", "generic_name": "cefazolin", "labeler_name": "Henry Schein Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "225 mg/mL"}], "application_number": "ANDA065047", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}