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Mirtazapine - 0615-5572-05 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 0615-5572
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: 0615-5572
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076122
Marketing Category: ANDA
Start Marketing Date: 20091130

Package Information of Mirtazapine

Package NDC: 0615-5572-05
Package Description: 15 TABLET in 1 BLISTER PACK (0615-5572-05)

NDC Information of Mirtazapine

NDC Code 0615-5572-05
Proprietary Name Mirtazapine
Package Description 15 TABLET in 1 BLISTER PACK (0615-5572-05)
Product NDC 0615-5572
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091130
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information