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ziprasidone hydrochloride - 0781-2166-60 - (ziprasidone hydrochloride)

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Drug Information of ziprasidone hydrochloride

Product NDC: 0781-2166
Proprietary Name: ziprasidone hydrochloride
Non Proprietary Name: ziprasidone hydrochloride
Active Ingredient(s): 40    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: 0781-2166
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077562
Marketing Category: ANDA
Start Marketing Date: 20130213

Package Information of ziprasidone hydrochloride

Package NDC: 0781-2166-60
Package Description: 60 CAPSULE in 1 BOTTLE (0781-2166-60)

NDC Information of ziprasidone hydrochloride

NDC Code 0781-2166-60
Proprietary Name ziprasidone hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (0781-2166-60)
Product NDC 0781-2166
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ziprasidone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130213
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of ziprasidone hydrochloride


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