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Mirtazapine - 0093-7304-65 - (Mirtazapine)

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Drug Information of Mirtazapine

Product NDC: 0093-7304
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 30    mg/1 & nbsp;   Mirtazapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Mirtazapine

Product NDC: 0093-7304
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076901
Marketing Category: ANDA
Start Marketing Date: 20050901

Package Information of Mirtazapine

Package NDC: 0093-7304-65
Package Description: 5 BLISTER PACK in 1 BOX (0093-7304-65) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-7304-18)

NDC Information of Mirtazapine

NDC Code 0093-7304-65
Proprietary Name Mirtazapine
Package Description 5 BLISTER PACK in 1 BOX (0093-7304-65) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-7304-18)
Product NDC 0093-7304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20050901
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name MIRTAZAPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information