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Selegiline Hydrochloride - 60505-3438-8 - (Selegiline Hydrochloride)

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Drug Information of Selegiline Hydrochloride

Product NDC: 60505-3438
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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Selegiline Hydrochloride

Product NDC: 60505-3438
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074871
Marketing Category: ANDA
Start Marketing Date: 19970706

Package Information of Selegiline Hydrochloride

Package NDC: 60505-3438-8
Package Description: 500 TABLET in 1 BOTTLE (60505-3438-8)

NDC Information of Selegiline Hydrochloride

NDC Code 60505-3438-8
Proprietary Name Selegiline Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (60505-3438-8)
Product NDC 60505-3438
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Selegiline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970706
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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