Home > National Drug Code (NDC) > Mirtazapine

Mirtazapine - 65862-021-90 - (Mirtazapine)

Alphabetical Index


Drug Information of Mirtazapine

Product NDC: 65862-021
Proprietary Name: Mirtazapine
Non Proprietary Name: Mirtazapine
Active Ingredient(s): 15    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: 65862-021
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077376
Marketing Category: ANDA
Start Marketing Date: 20051208

Package Information of Mirtazapine

Package NDC: 65862-021-90
Package Description: 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-021-90)

NDC Information of Mirtazapine

NDC Code 65862-021-90
Proprietary Name Mirtazapine
Package Description 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-021-90)
Product NDC 65862-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mirtazapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20051208
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name MIRTAZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mirtazapine


General Information