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Acebutolol Hydrochloride - 65162-669-50 - (Acebutolol Hydrochloride)

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Drug Information of Acebutolol Hydrochloride

Product NDC: 65162-669
Proprietary Name: Acebutolol Hydrochloride
Non Proprietary Name: Acebutolol Hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Acebutolol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Acebutolol Hydrochloride

Product NDC: 65162-669
Labeler Name: Amneal Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075047
Marketing Category: ANDA
Start Marketing Date: 20091201

Package Information of Acebutolol Hydrochloride

Package NDC: 65162-669-50
Package Description: 500 CAPSULE in 1 BOTTLE (65162-669-50)

NDC Information of Acebutolol Hydrochloride

NDC Code 65162-669-50
Proprietary Name Acebutolol Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (65162-669-50)
Product NDC 65162-669
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acebutolol Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals, LLC
Substance Name ACEBUTOLOL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Acebutolol Hydrochloride


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