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Methimazole - 0185-0205-01 - (Methimazole)

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Drug Information of Methimazole

Product NDC: 0185-0205
Proprietary Name: Methimazole
Non Proprietary Name: Methimazole
Active Ingredient(s): 5    mg/1 & nbsp;   Methimazole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methimazole

Product NDC: 0185-0205
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040411
Marketing Category: ANDA
Start Marketing Date: 20010327

Package Information of Methimazole

Package NDC: 0185-0205-01
Package Description: 100 TABLET in 1 BOTTLE (0185-0205-01)

NDC Information of Methimazole

NDC Code 0185-0205-01
Proprietary Name Methimazole
Package Description 100 TABLET in 1 BOTTLE (0185-0205-01)
Product NDC 0185-0205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methimazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010327
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name METHIMAZOLE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Thyroid Hormone Synthesis Inhibitor [EPC],Thyroid Hormone Synthesis Inhibitors [MoA]

Complete Information of Methimazole


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