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 330 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9834
Product ID 0404-9834_5c5cb92a-87b7-42e7-999c-d09323bfa0c3
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 04049834
Hyphenated Format 0404-9834

Supplemental Identifiers

RxCUI
1665050
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
  • 330 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9834-99) / 3 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (330 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5c5cb92a-87b7-42e7-999c-d09323bfa0c3", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["197d5702-2c20-480e-8246-4d0d21f871be"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9834-99)  / 3 mL in 1 VIAL", "package_ndc": "0404-9834-99", "marketing_start_date": "20220109"}], "brand_name": "CEFAZOLIN", "product_id": "0404-9834_5c5cb92a-87b7-42e7-999c-d09323bfa0c3", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0404-9834", "generic_name": "cefazolin", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "330 mg/mL"}], "application_number": "ANDA065047", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}