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Atomoxetine Hydrochloride - 47335-817-88 - (Atomoxetine Hydrochloride)

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Drug Information of Atomoxetine Hydrochloride

Product NDC: 47335-817
Proprietary Name: Atomoxetine Hydrochloride
Non Proprietary Name: Atomoxetine Hydrochloride
Active Ingredient(s): 40    mg/1 & nbsp;   Atomoxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Atomoxetine Hydrochloride

Product NDC: 47335-817
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079020
Marketing Category: ANDA
Start Marketing Date: 20101005

Package Information of Atomoxetine Hydrochloride

Package NDC: 47335-817-88
Package Description: 100 CAPSULE in 1 BOTTLE (47335-817-88)

NDC Information of Atomoxetine Hydrochloride

NDC Code 47335-817-88
Proprietary Name Atomoxetine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (47335-817-88)
Product NDC 47335-817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atomoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101005
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name ATOMOXETINE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of Atomoxetine Hydrochloride


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