Strattera - 0002-3238-07 - (Atomoxetine hydrochloride)

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Drug Information of Strattera

Product NDC: 0002-3238
Proprietary Name: Strattera
Non Proprietary Name: Atomoxetine hydrochloride
Active Ingredient(s): 18    mg/1 & nbsp;   Atomoxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Strattera

Product NDC: 0002-3238
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021411
Marketing Category: NDA
Start Marketing Date: 20030110

Package Information of Strattera

Package NDC: 0002-3238-07
Package Description: 7 CAPSULE in 1 BOTTLE (0002-3238-07)

NDC Information of Strattera

NDC Code 0002-3238-07
Proprietary Name Strattera
Package Description 7 CAPSULE in 1 BOTTLE (0002-3238-07)
Product NDC 0002-3238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atomoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030110
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name ATOMOXETINE HYDROCHLORIDE
Strength Number 18
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of Strattera


General Information