Strattera - 0002-5801-35 - (Atomoxetine hydrochloride)

Alphabetical Index


Drug Information of Strattera

Product NDC: 0002-5801
Proprietary Name: Strattera
Non Proprietary Name: Atomoxetine hydrochloride
Active Ingredient(s):    & nbsp;   Atomoxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Strattera

Product NDC: 0002-5801
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021411
Marketing Category: NDA
Start Marketing Date: 20090316

Package Information of Strattera

Package NDC: 0002-5801-35
Package Description: 1 KIT in 1 BLISTER PACK (0002-5801-35)

NDC Information of Strattera

NDC Code 0002-5801-35
Proprietary Name Strattera
Package Description 1 KIT in 1 BLISTER PACK (0002-5801-35)
Product NDC 0002-5801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atomoxetine hydrochloride
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20090316
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Strattera


General Information