cefazolin

Generic: cefazolin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler a-s medication solutions
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 330 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4256
Product ID 50090-4256_9f453c63-7855-47c4-9ac8-adb3cbe1bb26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065047
Listing Expiration 2026-12-31
Marketing Start 2001-09-18

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904256
Hyphenated Format 50090-4256

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
  • 25 VIAL in 1 BOX (50090-4256-0) / 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": "9f453c63-7855-47c4-9ac8-adb3cbe1bb26", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["8a772acc-726d-40e6-88ee-b6075cbf9b28"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 BOX (50090-4256-0)  / 3 mL in 1 VIAL", "package_ndc": "50090-4256-0", "marketing_start_date": "20190405"}], "brand_name": "Cefazolin", "product_id": "50090-4256_9f453c63-7855-47c4-9ac8-adb3cbe1bb26", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-4256", "generic_name": "Cefazolin", "labeler_name": "A-S Medication Solutions", "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": "20010918", "listing_expiration_date": "20261231"}