Geodon - 21695-060-10 - (ziprasidone hydrochloride)

Alphabetical Index


Drug Information of Geodon

Product NDC: 21695-060
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: 21695-060
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020825
Marketing Category: NDA
Start Marketing Date: 20010205

Package Information of Geodon

Package NDC: 21695-060-10
Package Description: 10 CAPSULE in 1 BOTTLE (21695-060-10)

NDC Information of Geodon

NDC Code 21695-060-10
Proprietary Name Geodon
Package Description 10 CAPSULE in 1 BOTTLE (21695-060-10)
Product NDC 21695-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ziprasidone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010205
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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