Ceftriaxone

Product NDC
60505-0753
11-digit product format
605050753
Labeler code
60505
Product ID
60505-0753_faa4586e-499f-4a88-8047-41e5f042eb62
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ceftriaxone
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Apotex Corporation
Application
ANDA065230
Marketing category
ANDA
Marketing start
2005-08-02
Marketing end
0000-00-00
Substance
CEFTRIAXONE SODIUM
Active strength
2 g/1
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-0753-3EA - Each60505-0753a2bd9fdc-658c-428d-b079-23357cb568c412015-12-02
60505-0753-4EA - Each60505-0753c87d9f11-961b-41b4-880e-7cc0e17fe06e12012-07-24