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MIRTAZAPINE - 54868-5642-0 - (Mirtazapine)

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Drug Information of MIRTAZAPINE

Product NDC: 54868-5642
Proprietary Name: MIRTAZAPINE
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 15    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of MIRTAZAPINE

Product NDC: 54868-5642
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076122
Marketing Category: ANDA
Start Marketing Date: 20060714

Package Information of MIRTAZAPINE

Package NDC: 54868-5642-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5642-0)

NDC Information of MIRTAZAPINE

NDC Code 54868-5642-0
Proprietary Name MIRTAZAPINE
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5642-0)
Product NDC 54868-5642
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060714
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of MIRTAZAPINE


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