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SOTALOL HYDROCHLORIDE - 0115-2722-02 - (SOTALOL HYDROCHLORIDE)

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Drug Information of SOTALOL HYDROCHLORIDE

Product NDC: 0115-2722
Proprietary Name: SOTALOL HYDROCHLORIDE
Non Proprietary Name: SOTALOL HYDROCHLORIDE
Active Ingredient(s): 120    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: 0115-2722
Labeler Name: Global Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075663
Marketing Category: ANDA
Start Marketing Date: 20001107

Package Information of SOTALOL HYDROCHLORIDE

Package NDC: 0115-2722-02
Package Description: 500 TABLET in 1 BOTTLE (0115-2722-02)

NDC Information of SOTALOL HYDROCHLORIDE

NDC Code 0115-2722-02
Proprietary Name SOTALOL HYDROCHLORIDE
Package Description 500 TABLET in 1 BOTTLE (0115-2722-02)
Product NDC 0115-2722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SOTALOL HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20001107
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals
Substance Name SOTALOL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of SOTALOL HYDROCHLORIDE


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