Cymbalta - 54868-5215-0 - (Duloxetine hydrochloride)

Alphabetical Index


Drug Information of Cymbalta

Product NDC: 54868-5215
Proprietary Name: Cymbalta
Non Proprietary Name: Duloxetine hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   Duloxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Cymbalta

Product NDC: 54868-5215
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021427
Marketing Category: NDA
Start Marketing Date: 20080428

Package Information of Cymbalta

Package NDC: 54868-5215-0
Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (54868-5215-0)

NDC Information of Cymbalta

NDC Code 54868-5215-0
Proprietary Name Cymbalta
Package Description 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (54868-5215-0)
Product NDC 54868-5215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Duloxetine hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080428
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name DULOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Cymbalta


General Information