Cymbalta - 50436-9982-1 - (Duloxetine hydrochloride)

Alphabetical Index


Drug Information of Cymbalta

Product NDC: 50436-9982
Proprietary Name: Cymbalta
Non Proprietary Name: Duloxetine hydrochloride
Active Ingredient(s): 60    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: 50436-9982
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021427
Marketing Category: NDA
Start Marketing Date: 20100115

Package Information of Cymbalta

Package NDC: 50436-9982-1
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50436-9982-1)

NDC Information of Cymbalta

NDC Code 50436-9982-1
Proprietary Name Cymbalta
Package Description 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50436-9982-1)
Product NDC 50436-9982
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Duloxetine hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100115
Marketing Category Name NDA
Labeler Name Unit Dose Services
Substance Name DULOXETINE HYDROCHLORIDE
Strength Number 60
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