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METHIMAZOLE - 64376-656-01 - (METHIMAZOLE)

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Drug Information of METHIMAZOLE

Product NDC: 64376-656
Proprietary Name: METHIMAZOLE
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 METHIMAZOLE

Product NDC: 64376-656
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202068
Marketing Category: ANDA
Start Marketing Date: 20120307

Package Information of METHIMAZOLE

Package NDC: 64376-656-01
Package Description: 100 TABLET in 1 BOTTLE (64376-656-01)

NDC Information of METHIMAZOLE

NDC Code 64376-656-01
Proprietary Name METHIMAZOLE
Package Description 100 TABLET in 1 BOTTLE (64376-656-01)
Product NDC 64376-656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHIMAZOLE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120307
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, 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 METHIMAZOLE


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