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Mirtazapine - 55154-8296-7 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 55154-8296
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: 55154-8296
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076119
Marketing Category: ANDA
Start Marketing Date: 20030129

Package Information of Mirtazapine

Package NDC: 55154-8296-7
Package Description: 14 TABLET, FILM COATED in 1 BLISTER PACK (55154-8296-7)

NDC Information of Mirtazapine

NDC Code 55154-8296-7
Proprietary Name Mirtazapine
Package Description 14 TABLET, FILM COATED in 1 BLISTER PACK (55154-8296-7)
Product NDC 55154-8296
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030129
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information