Cephalexin - 59834-202-17 - (Cephalexin)

Alphabetical Index


Drug Information of Cephalexin

Product NDC: 59834-202
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 125    mg/5mL & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 59834-202
Labeler Name: OrchidPharma Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065326
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Cephalexin

Package NDC: 59834-202-17
Package Description: 100 mL in 1 BOTTLE (59834-202-17)

NDC Information of Cephalexin

NDC Code 59834-202-17
Proprietary Name Cephalexin
Package Description 100 mL in 1 BOTTLE (59834-202-17)
Product NDC 59834-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name OrchidPharma Inc
Substance Name CEPHALEXIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information