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Phenelzine Sulfate - 43386-360-21 - (Phenelzine Sulfate)

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Drug Information of Phenelzine Sulfate

Product NDC: 43386-360
Proprietary Name: Phenelzine Sulfate
Non Proprietary Name: Phenelzine Sulfate
Active Ingredient(s): 15    mg/1 & nbsp;   Phenelzine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phenelzine Sulfate

Product NDC: 43386-360
Labeler Name: GAVIS Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200181
Marketing Category: ANDA
Start Marketing Date: 20101214

Package Information of Phenelzine Sulfate

Package NDC: 43386-360-21
Package Description: 60 TABLET in 1 BOTTLE (43386-360-21)

NDC Information of Phenelzine Sulfate

NDC Code 43386-360-21
Proprietary Name Phenelzine Sulfate
Package Description 60 TABLET in 1 BOTTLE (43386-360-21)
Product NDC 43386-360
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenelzine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101214
Marketing Category Name ANDA
Labeler Name GAVIS Pharmaceuticals, LLC
Substance Name PHENELZINE SULFATE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA]

Complete Information of Phenelzine Sulfate


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