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Mirtazapine - 49349-396-02 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 49349-396
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: 49349-396
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076921
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Mirtazapine

Package NDC: 49349-396-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-396-02)

NDC Information of Mirtazapine

NDC Code 49349-396-02
Proprietary Name Mirtazapine
Package Description 30 TABLET in 1 BLISTER PACK (49349-396-02)
Product NDC 49349-396
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name MIRTAZAPINE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


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