cefazolin
Generic: cefazolin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
proficient rx lp
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-679
Product ID
71205-679_d24529e3-e2b4-46d6-81ba-b7da74501792
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
71205679
Hyphenated Format
71205-679
Supplemental Identifiers
RxCUI
UPC
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 VIAL, SINGLE-DOSE in 1 BOX (71205-679-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "d24529e3-e2b4-46d6-81ba-b7da74501792", "openfda": {"upc": ["0371205679019"], "unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["d24529e3-e2b4-46d6-81ba-b7da74501792"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BOX (71205-679-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "71205-679-01", "marketing_start_date": "20220801"}], "brand_name": "Cefazolin", "product_id": "71205-679_d24529e3-e2b4-46d6-81ba-b7da74501792", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71205-679", "generic_name": "Cefazolin", "labeler_name": "Proficient Rx LP", "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"}