Geodon - 54868-4544-0 - (ziprasidone hydrochloride)

Alphabetical Index


Drug Information of Geodon

Product NDC: 54868-4544
Proprietary Name: Geodon
Non Proprietary Name: ziprasidone hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   ziprasidone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Geodon

Product NDC: 54868-4544
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020825
Marketing Category: NDA
Start Marketing Date: 20051011

Package Information of Geodon

Package NDC: 54868-4544-0
Package Description: 60 CAPSULE in 1 BOTTLE (54868-4544-0)

NDC Information of Geodon

NDC Code 54868-4544-0
Proprietary Name Geodon
Package Description 60 CAPSULE in 1 BOTTLE (54868-4544-0)
Product NDC 54868-4544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ziprasidone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20051011
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of Geodon


General Information