cefazolin

Generic: cefazolin

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler sandoz inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS PARENTERAL
Active Ingredients

cefazolin sodium 1 g/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3451
Product ID 0781-3451_05cd44b2-275f-44f5-b4f8-22393df834a1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062831
Listing Expiration 2027-12-31
Marketing Start 1988-12-09

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813451
Hyphenated Format 0781-3451

Supplemental Identifiers

RxCUI
1665050 1665052
UNII
P380M0454Z

Packaging Origin

Original Packager
true

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 ANDA062831 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS PARENTERAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (0781-3451-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70)
  • 25 VIAL in 1 CARTON (0781-3451-96) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70)
source: ndc

Packages (2)

0781-3451-95 10 VIAL in 1 CARTON (0781-3451-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70) 0781-3451-96 25 VIAL in 1 CARTON (0781-3451-96) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70)

Ingredients (1)

cefazolin sodium (1 g/1)

Linked Drug Pages (1)

Cefazolin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "PARENTERAL"], "spl_id": "05cd44b2-275f-44f5-b4f8-22393df834a1", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665052"], "spl_set_id": ["18e7366a-1b3e-4010-8f4a-dd559d4f2146"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0781-3451-95)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70)", "package_ndc": "0781-3451-95", "marketing_start_date": "20260105"}, {"sample": false, "description": "25 VIAL in 1 CARTON (0781-3451-96)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3451-70)", "package_ndc": "0781-3451-96", "marketing_start_date": "19881209"}], "brand_name": "Cefazolin", "product_id": "0781-3451_05cd44b2-275f-44f5-b4f8-22393df834a1", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-3451", "generic_name": "Cefazolin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA062831", "marketing_category": "ANDA", "marketing_start_date": "19881209", "listing_expiration_date": "20271231"}