cefazolin sodium

Generic: cefazolin sodium

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin sodium
Generic Name cefazolin sodium
Labeler direct_rx
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 1 g/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-584
Product ID 72189-584_22dfc2e4-07a8-8d13-e063-6394a90a3e9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203661
Listing Expiration 2026-12-31
Marketing Start 2024-09-24

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189584
Hyphenated Format 72189-584

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 sodium (source: ndc)
Generic Name cefazolin sodium (source: ndc)
Application Number ANDA203661 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01)
source: ndc

Packages (1)

72189-584-01 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01)

Ingredients (1)

cefazolin sodium (1 g/1)

Linked Drug Pages (1)

Cefazolin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "22dfc2e4-07a8-8d13-e063-6394a90a3e9f", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["22dfc2e4-07a7-8d13-e063-6394a90a3e9f"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (72189-584-01)", "package_ndc": "72189-584-01", "marketing_start_date": "20240924"}], "brand_name": "Cefazolin Sodium", "product_id": "72189-584_22dfc2e4-07a8-8d13-e063-6394a90a3e9f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72189-584", "generic_name": "Cefazolin Sodium", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin Sodium", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20240924", "listing_expiration_date": "20261231"}