Cefadroxil

Product NDC
68289-014
11-digit product format
682890014
Labeler code
68289
Product ID
68289-014_f219e051-99c0-4142-8bd8-269b049e9722
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cefadroxil
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
Jazeera Pharmaceutical
Application
ANDA091036
Marketing category
ANDA
Marketing start
2012-11-28
Marketing end
0000-00-00
Substance
CEFADROXIL
Active strength
500 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#