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Ziprasidone Hydrochloride - 68084-581-09 - (Ziprasidone Hydrochloride)

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Drug Information of Ziprasidone Hydrochloride

Product NDC: 68084-581
Proprietary Name: Ziprasidone Hydrochloride
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 Ziprasidone Hydrochloride

Product NDC: 68084-581
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077560
Marketing Category: ANDA
Start Marketing Date: 20130702

Package Information of Ziprasidone Hydrochloride

Package NDC: 68084-581-09
Package Description: 8 BLISTER PACK in 1 CARTON (68084-581-09) > 10 CAPSULE in 1 BLISTER PACK (68084-581-11)

NDC Information of Ziprasidone Hydrochloride

NDC Code 68084-581-09
Proprietary Name Ziprasidone Hydrochloride
Package Description 8 BLISTER PACK in 1 CARTON (68084-581-09) > 10 CAPSULE in 1 BLISTER PACK (68084-581-11)
Product NDC 68084-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ziprasidone Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130702
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of Ziprasidone Hydrochloride


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