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Selegiline Hydrochloride - 0378-9290-91 - (selegiline hydrochloride)

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Drug Information of Selegiline Hydrochloride

Product NDC: 0378-9290
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: 0378-9290
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074866
Marketing Category: ANDA
Start Marketing Date: 20100308

Package Information of Selegiline Hydrochloride

Package NDC: 0378-9290-91
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (0378-9290-91)

NDC Information of Selegiline Hydrochloride

NDC Code 0378-9290-91
Proprietary Name Selegiline Hydrochloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (0378-9290-91)
Product NDC 0378-9290
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name selegiline hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100308
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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