cefazolin
Generic: cefazolin sodium
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin sodium
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
cefazolin sodium 1 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-3503
Product ID
0338-3503_b0e63b97-7941-485b-bd92-98cbd0fc1b71
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA207131
Listing Expiration
2026-12-31
Marketing Start
2015-08-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03383503
Hyphenated Format
0338-3503
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 sodium (source: ndc)
Application Number
NDA207131 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/50mL
Packaging
- 24 BAG in 1 CARTON (0338-3503-41) / 50 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b0e63b97-7941-485b-bd92-98cbd0fc1b71", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665060", "2630753"], "spl_set_id": ["d91a8d13-99a0-4d87-88dc-71cbd37922b4"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-3503-41) / 50 mL in 1 BAG", "package_ndc": "0338-3503-41", "marketing_start_date": "20150807"}], "brand_name": "Cefazolin", "product_id": "0338-3503_b0e63b97-7941-485b-bd92-98cbd0fc1b71", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0338-3503", "generic_name": "Cefazolin Sodium", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/50mL"}], "application_number": "NDA207131", "marketing_category": "NDA", "marketing_start_date": "20150807", "listing_expiration_date": "20261231"}