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Ziprasidone hydrochloride - 55648-991-06 - (Ziprasidone hydrochloride)

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Drug Information of Ziprasidone hydrochloride

Product NDC: 55648-991
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: 55648-991
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090348
Marketing Category: ANDA
Start Marketing Date: 20120901

Package Information of Ziprasidone hydrochloride

Package NDC: 55648-991-06
Package Description: 10 BLISTER PACK in 1 CARTON (55648-991-06) > 8 CAPSULE in 1 BLISTER PACK

NDC Information of Ziprasidone hydrochloride

NDC Code 55648-991-06
Proprietary Name Ziprasidone hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (55648-991-06) > 8 CAPSULE in 1 BLISTER PACK
Product NDC 55648-991
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ziprasidone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120901
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of Ziprasidone hydrochloride


General Information