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Mirtazapine - 63739-355-10 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 63739-355
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 15    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: 63739-355
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076119
Marketing Category: ANDA
Start Marketing Date: 20070807

Package Information of Mirtazapine

Package NDC: 63739-355-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-355-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Mirtazapine

NDC Code 63739-355-10
Proprietary Name Mirtazapine
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-355-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-355
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070807
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


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