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Mirtazapine - 54868-6384-0 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 54868-6384
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 45    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Mirtazapine

Product NDC: 54868-6384
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021208
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20121207

Package Information of Mirtazapine

Package NDC: 54868-6384-0
Package Description: 5 BLISTER PACK in 1 BOX (54868-6384-0) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Mirtazapine

NDC Code 54868-6384-0
Proprietary Name Mirtazapine
Package Description 5 BLISTER PACK in 1 BOX (54868-6384-0) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 54868-6384
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20121207
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name MIRTAZAPINE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information