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Betapace AF - 50419-116-06 - (sotalol hydrochloride)

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Drug Information of Betapace AF

Product NDC: 50419-116
Proprietary Name: Betapace AF
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 Betapace AF

Product NDC: 50419-116
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021151
Marketing Category: NDA
Start Marketing Date: 20000222

Package Information of Betapace AF

Package NDC: 50419-116-06
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE (50419-116-06) > 60 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Betapace AF

NDC Code 50419-116-06
Proprietary Name Betapace AF
Package Description 1 BOTTLE, PLASTIC in 1 PACKAGE (50419-116-06) > 60 TABLET in 1 BOTTLE, PLASTIC
Product NDC 50419-116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sotalol hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000222
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name SOTALOL HYDROCHLORIDE
Strength Number 160
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Betapace AF


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