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Acebutolol Hydrochloride - 54868-4216-0 - (Acebutolol Hydrochloride)

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Drug Information of Acebutolol Hydrochloride

Product NDC: 54868-4216
Proprietary Name: Acebutolol Hydrochloride
Non Proprietary Name: Acebutolol Hydrochloride
Active Ingredient(s): 400    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: 54868-4216
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075047
Marketing Category: ANDA
Start Marketing Date: 20050422

Package Information of Acebutolol Hydrochloride

Package NDC: 54868-4216-0
Package Description: 30 CAPSULE in 1 BOTTLE (54868-4216-0)

NDC Information of Acebutolol Hydrochloride

NDC Code 54868-4216-0
Proprietary Name Acebutolol Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (54868-4216-0)
Product NDC 54868-4216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acebutolol Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050422
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACEBUTOLOL HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Acebutolol Hydrochloride


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