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Ethambutol Hydrochloride - 54879-002-00 - (Ethambutol Hydrochloride)

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Drug Information of Ethambutol Hydrochloride

Product NDC: 54879-002
Proprietary Name: Ethambutol Hydrochloride
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 Hydrochloride

Product NDC: 54879-002
Labeler Name: STI Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016320
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20061215

Package Information of Ethambutol Hydrochloride

Package NDC: 54879-002-00
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (54879-002-00) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ethambutol Hydrochloride

NDC Code 54879-002-00
Proprietary Name Ethambutol Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (54879-002-00) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 54879-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethambutol Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061215
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name STI Pharma LLC
Substance Name ETHAMBUTOL HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Ethambutol Hydrochloride


General Information