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mirtazapine - 0185-0212-05 - (mirtazapine)

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Drug Information of mirtazapine

Product NDC: 0185-0212
Proprietary Name: mirtazapine
Non Proprietary Name: mirtazapine
Active Ingredient(s): 30    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: 0185-0212
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076219
Marketing Category: ANDA
Start Marketing Date: 20030619

Package Information of mirtazapine

Package NDC: 0185-0212-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0185-0212-05)

NDC Information of mirtazapine

NDC Code 0185-0212-05
Proprietary Name mirtazapine
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0185-0212-05)
Product NDC 0185-0212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030619
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name MIRTAZAPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of mirtazapine


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