Ethambutol - 61748-014-06 - (Ethambutol hydrochloride)

Alphabetical Index


Drug Information of Ethambutol

Product NDC: 61748-014
Proprietary Name: Ethambutol
Non Proprietary Name: Ethambutol hydrochloride
Active Ingredient(s): 400    mg/1 & nbsp;   Ethambutol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ethambutol

Product NDC: 61748-014
Labeler Name: Versa Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075095
Marketing Category: ANDA
Start Marketing Date: 19991201

Package Information of Ethambutol

Package NDC: 61748-014-06
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61748-014-06)

NDC Information of Ethambutol

NDC Code 61748-014-06
Proprietary Name Ethambutol
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61748-014-06)
Product NDC 61748-014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethambutol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19991201
Marketing Category Name ANDA
Labeler Name Versa Pharmaceutical
Substance Name ETHAMBUTOL HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Ethambutol


General Information