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Mirtazapine - 55154-5680-0 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 55154-5680
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 30    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mirtazapine

Product NDC: 55154-5680
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076122
Marketing Category: ANDA
Start Marketing Date: 20091130

Package Information of Mirtazapine

Package NDC: 55154-5680-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5680-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Mirtazapine

NDC Code 55154-5680-0
Proprietary Name Mirtazapine
Package Description 10 BLISTER PACK in 1 BAG (55154-5680-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5680
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 Cardinal Health
Substance Name MIRTAZAPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


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