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Mirtazapine - 21695-082-30 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 21695-082
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: 21695-082
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076921
Marketing Category: ANDA
Start Marketing Date: 20041022

Package Information of Mirtazapine

Package NDC: 21695-082-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-082-30)

NDC Information of Mirtazapine

NDC Code 21695-082-30
Proprietary Name Mirtazapine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-082-30)
Product NDC 21695-082
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041022
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name MIRTAZAPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


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