GEODON - 24236-267-21 - (ZIPRASIDONE HYDROCHLORIDE)

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Drug Information of GEODON

Product NDC: 24236-267
Proprietary Name: GEODON
Non Proprietary Name: ZIPRASIDONE HYDROCHLORIDE
Active Ingredient(s): 60    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: 24236-267
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020825
Marketing Category: NDA
Start Marketing Date: 20101220

Package Information of GEODON

Package NDC: 24236-267-21
Package Description: 120 CAPSULE in 1 CANISTER (24236-267-21)

NDC Information of GEODON

NDC Code 24236-267-21
Proprietary Name GEODON
Package Description 120 CAPSULE in 1 CANISTER (24236-267-21)
Product NDC 24236-267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ZIPRASIDONE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101220
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of GEODON


General Information