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Mirtazapine - 51079-088-56 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 51079-088
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 45    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mirtazapine

Product NDC: 51079-088
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076122
Marketing Category: ANDA
Start Marketing Date: 20111109

Package Information of Mirtazapine

Package NDC: 51079-088-56
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-088-56) > 30 TABLET in 1 BLISTER PACK (51079-088-30)

NDC Information of Mirtazapine

NDC Code 51079-088-56
Proprietary Name Mirtazapine
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-088-56) > 30 TABLET in 1 BLISTER PACK (51079-088-30)
Product NDC 51079-088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111109
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name MIRTAZAPINE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information