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Ethambutol Hydrochloride - 49349-446-02 - (Ethambutol Hydrochloride)

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Drug Information of Ethambutol Hydrochloride

Product NDC: 49349-446
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: 49349-446
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075095
Marketing Category: ANDA
Start Marketing Date: 20110801

Package Information of Ethambutol Hydrochloride

Package NDC: 49349-446-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-446-02)

NDC Information of Ethambutol Hydrochloride

NDC Code 49349-446-02
Proprietary Name Ethambutol Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-446-02)
Product NDC 49349-446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ethambutol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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