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Methimazole - 68084-275-01 - (Methimazole)

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Drug Information of Methimazole

Product NDC: 68084-275
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: 68084-275
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040411
Marketing Category: ANDA
Start Marketing Date: 20130614

Package Information of Methimazole

Package NDC: 68084-275-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-275-01) > 10 TABLET in 1 BLISTER PACK (68084-275-11)

NDC Information of Methimazole

NDC Code 68084-275-01
Proprietary Name Methimazole
Package Description 10 BLISTER PACK in 1 CARTON (68084-275-01) > 10 TABLET in 1 BLISTER PACK (68084-275-11)
Product NDC 68084-275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methimazole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130614
Marketing Category Name ANDA
Labeler Name American Health Packaging
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


General Information