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Mirtazapine - 58118-1117-9 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 58118-1117
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: 58118-1117
Labeler Name: Clinical Solutions Wholesale
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076312
Marketing Category: ANDA
Start Marketing Date: 20030619

Package Information of Mirtazapine

Package NDC: 58118-1117-9
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-1117-9)

NDC Information of Mirtazapine

NDC Code 58118-1117-9
Proprietary Name Mirtazapine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-1117-9)
Product NDC 58118-1117
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 Clinical Solutions Wholesale
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information