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Mirtazapine - 60505-0249-3 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 60505-0249
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 45    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: 60505-0249
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077666
Marketing Category: ANDA
Start Marketing Date: 20070822

Package Information of Mirtazapine

Package NDC: 60505-0249-3
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60505-0249-3)

NDC Information of Mirtazapine

NDC Code 60505-0249-3
Proprietary Name Mirtazapine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60505-0249-3)
Product NDC 60505-0249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070822
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name MIRTAZAPINE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information