Ceftriaxone

Product NDC
63323-348
11-digit product format
633230348
Labeler code
63323
Product ID
63323-348_7e06a355-f45b-4e3c-e053-2a91aa0aeb9d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ceftriaxone
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS
Labeler
Fresenius Kabi USA, LLC
Application
ANDA065328
Marketing category
ANDA
Marketing start
2011-06-20
Marketing end
0000-00-00
Substance
CEFTRIAXONE 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
63323-348-61EA - Each63323-34826620246-0c12-41a2-9f14-2ba7ccb8336c12012-07-24