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Mirtazapine - 50436-3897-2 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 50436-3897
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 15    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mirtazapine

Product NDC: 50436-3897
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076312
Marketing Category: ANDA
Start Marketing Date: 20030619

Package Information of Mirtazapine

Package NDC: 50436-3897-2
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (50436-3897-2)

NDC Information of Mirtazapine

NDC Code 50436-3897-2
Proprietary Name Mirtazapine
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (50436-3897-2)
Product NDC 50436-3897
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030619
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information