TAPAZOLE - 60793-105-01 - (methimazole)

Alphabetical Index


Drug Information of TAPAZOLE

Product NDC: 60793-105
Proprietary Name: TAPAZOLE
Non Proprietary Name: methimazole
Active Ingredient(s): 10    mg/1 & nbsp;   methimazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TAPAZOLE

Product NDC: 60793-105
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040320
Marketing Category: ANDA
Start Marketing Date: 20000331

Package Information of TAPAZOLE

Package NDC: 60793-105-01
Package Description: 100 TABLET in 1 BOTTLE (60793-105-01)

NDC Information of TAPAZOLE

NDC Code 60793-105-01
Proprietary Name TAPAZOLE
Package Description 100 TABLET in 1 BOTTLE (60793-105-01)
Product NDC 60793-105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methimazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000331
Marketing Category Name ANDA
Labeler Name King Pharmaceuticals, Inc.
Substance Name METHIMAZOLE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Thyroid Hormone Synthesis Inhibitor [EPC],Thyroid Hormone Synthesis Inhibitors [MoA]

Complete Information of TAPAZOLE


General Information