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Sotalol Hydrochloride - 60505-0223-2 - (Sotalol Hydrochloride)

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Drug Information of Sotalol Hydrochloride

Product NDC: 60505-0223
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: 60505-0223
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076214
Marketing Category: ANDA
Start Marketing Date: 20030909

Package Information of Sotalol Hydrochloride

Package NDC: 60505-0223-2
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (60505-0223-2)

NDC Information of Sotalol Hydrochloride

NDC Code 60505-0223-2
Proprietary Name Sotalol Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (60505-0223-2)
Product NDC 60505-0223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sotalol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030909
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name SOTALOL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Sotalol Hydrochloride


General Information