SARAFEM - 0430-0220-14 - (fluoxetine hydrochloride)

Alphabetical Index


Drug Information of SARAFEM

Product NDC: 0430-0220
Proprietary Name: SARAFEM
Non Proprietary Name: fluoxetine hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   fluoxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SARAFEM

Product NDC: 0430-0220
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021860
Marketing Category: NDA
Start Marketing Date: 20080624

Package Information of SARAFEM

Package NDC: 0430-0220-14
Package Description: 72 CARTON in 1 CASE (0430-0220-14) > 4 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK

NDC Information of SARAFEM

NDC Code 0430-0220-14
Proprietary Name SARAFEM
Package Description 72 CARTON in 1 CASE (0430-0220-14) > 4 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK
Product NDC 0430-0220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080624
Marketing Category Name NDA
Labeler Name Warner Chilcott (US), LLC
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of SARAFEM


General Information