Home > National Drug Code (NDC) > ziprasidone hydrochloride

ziprasidone hydrochloride - 60505-2529-8 - (Ziprasidone HCl)

Alphabetical Index


Drug Information of ziprasidone hydrochloride

Product NDC: 60505-2529
Proprietary Name: ziprasidone hydrochloride
Non Proprietary Name: Ziprasidone HCl
Active Ingredient(s): 40    mg/1 & nbsp;   Ziprasidone HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ziprasidone hydrochloride

Product NDC: 60505-2529
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077561
Marketing Category: ANDA
Start Marketing Date: 20120514

Package Information of ziprasidone hydrochloride

Package NDC: 60505-2529-8
Package Description: 1000 CAPSULE in 1 BOTTLE (60505-2529-8)

NDC Information of ziprasidone hydrochloride

NDC Code 60505-2529-8
Proprietary Name ziprasidone hydrochloride
Package Description 1000 CAPSULE in 1 BOTTLE (60505-2529-8)
Product NDC 60505-2529
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ziprasidone HCl
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120514
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ZIPRASIDONE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC]

Complete Information of ziprasidone hydrochloride


General Information