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sotalol hydrochloride - 54868-5549-1 - (sotalol hydrochloride)

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Drug Information of sotalol hydrochloride

Product NDC: 54868-5549
Proprietary Name: sotalol hydrochloride
Non Proprietary Name: sotalol hydrochloride
Active Ingredient(s): 160    mg/1 & nbsp;   sotalol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of sotalol hydrochloride

Product NDC: 54868-5549
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075366
Marketing Category: ANDA
Start Marketing Date: 20060314

Package Information of sotalol hydrochloride

Package NDC: 54868-5549-1
Package Description: 20 TABLET in 1 BOTTLE (54868-5549-1)

NDC Information of sotalol hydrochloride

NDC Code 54868-5549-1
Proprietary Name sotalol hydrochloride
Package Description 20 TABLET in 1 BOTTLE (54868-5549-1)
Product NDC 54868-5549
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sotalol hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060314
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name SOTALOL HYDROCHLORIDE
Strength Number 160
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of sotalol hydrochloride


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