Cephalexin - 61442-202-01 - (Cephalexin)

Alphabetical Index


Drug Information of Cephalexin

Product NDC: 61442-202
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/5mL & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 61442-202
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065336
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Cephalexin

Package NDC: 61442-202-01
Package Description: 24 BOTTLE in 1 BOX (61442-202-01) > 100 mL in 1 BOTTLE

NDC Information of Cephalexin

NDC Code 61442-202-01
Proprietary Name Cephalexin
Package Description 24 BOTTLE in 1 BOX (61442-202-01) > 100 mL in 1 BOTTLE
Product NDC 61442-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name CEPHALEXIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cephalexin


General Information