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 1 g/1

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9833
Product ID 0404-9833_b7d89e4d-5b66-41d1-9a36-10c57cf0a5b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203661
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 04049833
Hyphenated Format 0404-9833

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 ANDA203661 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9833-99) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (1 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "b7d89e4d-5b66-41d1-9a36-10c57cf0a5b2", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["5a8c4bb2-a75e-4d7d-91fb-9a95f04fc94b"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9833-99)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9833-99", "marketing_start_date": "20220109"}], "brand_name": "CEFAZOLIN", "product_id": "0404-9833_b7d89e4d-5b66-41d1-9a36-10c57cf0a5b2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0404-9833", "generic_name": "cefazolin", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}