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Ziprasidone - 59762-2004-2 - (ziprasidone hydrochloride)

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Drug Information of Ziprasidone

Product NDC: 59762-2004
Proprietary Name: Ziprasidone
Non Proprietary Name: ziprasidone hydrochloride
Active Ingredient(s): 80    mg/1 & nbsp;   ziprasidone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ziprasidone

Product NDC: 59762-2004
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020825
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20010205

Package Information of Ziprasidone

Package NDC: 59762-2004-2
Package Description: 500 CAPSULE in 1 BOTTLE (59762-2004-2)

NDC Information of Ziprasidone

NDC Code 59762-2004-2
Proprietary Name Ziprasidone
Package Description 500 CAPSULE in 1 BOTTLE (59762-2004-2)
Product NDC 59762-2004
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 AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of Ziprasidone


General Information