cefazolin
Generic: cefazolin
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
sandoz inc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3452
Product ID
0781-3452_c888c95b-df82-4261-854e-f74f9b2179e1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062831
Listing Expiration
2026-12-31
Marketing Start
1988-12-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813452
Hyphenated Format
0781-3452
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 g/1
Packaging
- 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3452-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-3452-46)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "PARENTERAL"], "spl_id": "c888c95b-df82-4261-854e-f74f9b2179e1", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["313920"], "spl_set_id": ["e58f87fb-a47d-4081-a454-e4e916e2f629"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3452-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-3452-46)", "package_ndc": "0781-3452-95", "marketing_start_date": "19881209"}], "brand_name": "Cefazolin", "product_id": "0781-3452_c888c95b-df82-4261-854e-f74f9b2179e1", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-3452", "generic_name": "Cefazolin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA062831", "marketing_category": "ANDA", "marketing_start_date": "19881209", "listing_expiration_date": "20261231"}