Cefazolin

Product NDC
60505-6094
11-digit product format
605056094
Labeler code
60505
Product ID
60505-6094_75247770-da12-442e-a1a6-f293f52ede97
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefazolin
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS
Labeler
Apotex Corporation
Application
ANDA065247
Marketing category
ANDA
Marketing start
2012-04-20
Marketing end
0000-00-00
Substance
CEFAZOLIN SODIUM
Active strength
10 g/1
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-6094-0EA - Each60505-6094a64d6113-ff24-46cf-97bf-d315212c67ab12013-02-13
60505-6094-1EA - Each60505-6094996dfe12-9c14-4753-b38d-31ab6ade0ba212016-05-16