Cymbalta - 55154-1818-0 - (Duloxetine hydrochloride)

Alphabetical Index


Drug Information of Cymbalta

Product NDC: 55154-1818
Proprietary Name: Cymbalta
Non Proprietary Name: Duloxetine hydrochloride
Active Ingredient(s): 30    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: 55154-1818
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021427
Marketing Category: NDA
Start Marketing Date: 20040824

Package Information of Cymbalta

Package NDC: 55154-1818-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1818-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Cymbalta

NDC Code 55154-1818-0
Proprietary Name Cymbalta
Package Description 10 BLISTER PACK in 1 BAG (55154-1818-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55154-1818
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Duloxetine hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20040824
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name DULOXETINE HYDROCHLORIDE
Strength Number 30
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