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Atomoxetine hydrochloride - 0781-2262-22 - (Atomoxetine hydrochloride)

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Drug Information of Atomoxetine hydrochloride

Product NDC: 0781-2262
Proprietary Name: Atomoxetine hydrochloride
Non Proprietary Name: Atomoxetine hydrochloride
Active Ingredient(s): 25    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: 0781-2262
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079018
Marketing Category: ANDA
Start Marketing Date: 20101215

Package Information of Atomoxetine hydrochloride

Package NDC: 0781-2262-22
Package Description: 2000 CAPSULE in 1 BOTTLE (0781-2262-22)

NDC Information of Atomoxetine hydrochloride

NDC Code 0781-2262-22
Proprietary Name Atomoxetine hydrochloride
Package Description 2000 CAPSULE in 1 BOTTLE (0781-2262-22)
Product NDC 0781-2262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atomoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101215
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ATOMOXETINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of Atomoxetine hydrochloride


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