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SELEGILINE HYDROCHLORIDE - 60505-0055-2 - (SELEGILINE HYDROCHLORIDE)

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Drug Information of SELEGILINE HYDROCHLORIDE

Product NDC: 60505-0055
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: 60505-0055
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075321
Marketing Category: ANDA
Start Marketing Date: 19970715

Package Information of SELEGILINE HYDROCHLORIDE

Package NDC: 60505-0055-2
Package Description: 1000 CAPSULE in 1 BOTTLE (60505-0055-2)

NDC Information of SELEGILINE HYDROCHLORIDE

NDC Code 60505-0055-2
Proprietary Name SELEGILINE HYDROCHLORIDE
Package Description 1000 CAPSULE in 1 BOTTLE (60505-0055-2)
Product NDC 60505-0055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SELEGILINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970715
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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