cefazolin
Generic: cefazolin
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
propharma distribution
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
84549-142
Product ID
84549-142_3d5cc73c-8a42-b285-e063-6294a90a609f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203661
Listing Expiration
2026-12-31
Marketing Start
2017-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549142
Hyphenated Format
84549-142
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (84549-142-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3d5cc73c-8a42-b285-e063-6294a90a609f", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["3d5cc73c-8a41-b285-e063-6294a90a609f"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (84549-142-05)", "package_ndc": "84549-142-05", "marketing_start_date": "20250901"}], "brand_name": "Cefazolin", "product_id": "84549-142_3d5cc73c-8a42-b285-e063-6294a90a609f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "84549-142", "generic_name": "Cefazolin", "labeler_name": "ProPharma Distribution", "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": "20170630", "listing_expiration_date": "20261231"}