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SELEGILINE HYDROCHLORIDE - 67253-700-06 - (SELEGILINE HYDROCHLORIDE)

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Drug Information of SELEGILINE HYDROCHLORIDE

Product NDC: 67253-700
Proprietary Name: SELEGILINE HYDROCHLORIDE
Non Proprietary Name: SELEGILINE HYDROCHLORIDE
Active Ingredient(s): 5    mg/1 & nbsp;   SELEGILINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of SELEGILINE HYDROCHLORIDE

Product NDC: 67253-700
Labeler Name: DAVA International Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075352
Marketing Category: ANDA
Start Marketing Date: 20061104

Package Information of SELEGILINE HYDROCHLORIDE

Package NDC: 67253-700-06
Package Description: 60 CAPSULE in 1 BOTTLE (67253-700-06)

NDC Information of SELEGILINE HYDROCHLORIDE

NDC Code 67253-700-06
Proprietary Name SELEGILINE HYDROCHLORIDE
Package Description 60 CAPSULE in 1 BOTTLE (67253-700-06)
Product NDC 67253-700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SELEGILINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20061104
Marketing Category Name ANDA
Labeler Name DAVA International Inc.
Substance Name SELEGILINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA]

Complete Information of SELEGILINE HYDROCHLORIDE


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