ALBENZA - 52054-550-28 - (albendazole)

Alphabetical Index


Drug Information of ALBENZA

Product NDC: 52054-550
Proprietary Name: ALBENZA
Non Proprietary Name: albendazole
Active Ingredient(s): 200    mg/1 & nbsp;   albendazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ALBENZA

Product NDC: 52054-550
Labeler Name: Amedra Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020666
Marketing Category: NDA
Start Marketing Date: 20111222

Package Information of ALBENZA

Package NDC: 52054-550-28
Package Description: 28 TABLET, FILM COATED in 1 BOTTLE (52054-550-28)

NDC Information of ALBENZA

NDC Code 52054-550-28
Proprietary Name ALBENZA
Package Description 28 TABLET, FILM COATED in 1 BOTTLE (52054-550-28)
Product NDC 52054-550
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albendazole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111222
Marketing Category Name NDA
Labeler Name Amedra Pharmaceuticals
Substance Name ALBENDAZOLE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antihelminthic [EPC]

Complete Information of ALBENZA


General Information