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Ethambutol Hydrochloride - 68180-281-13 - (Ethambutol Hydrochloride)

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Drug Information of Ethambutol Hydrochloride

Product NDC: 68180-281
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
Coding System: National Drug Codes(NDC)

Labeler Information of Ethambutol Hydrochloride

Product NDC: 68180-281
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078939
Marketing Category: ANDA
Start Marketing Date: 20090704

Package Information of Ethambutol Hydrochloride

Package NDC: 68180-281-13
Package Description: 4 BLISTER PACK in 1 CARTON (68180-281-13) > 14 TABLET in 1 BLISTER PACK (68180-281-11)

NDC Information of Ethambutol Hydrochloride

NDC Code 68180-281-13
Proprietary Name Ethambutol Hydrochloride
Package Description 4 BLISTER PACK in 1 CARTON (68180-281-13) > 14 TABLET in 1 BLISTER PACK (68180-281-11)
Product NDC 68180-281
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethambutol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090704
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
Substance Name ETHAMBUTOL HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Ethambutol Hydrochloride


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