cefazolin

Generic: cefazolin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler proficient rx lp
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 1 g/1

Manufacturer
Proficient Rx LP

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205679
Hyphenated Format 71205-679

Supplemental Identifiers

RxCUI
1665050
UPC
0371205679019
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 BOX (71205-679-01) / 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": "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"}