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ziprasidone hydrochloride - 55111-257-60 - (ziprasidone hydrochloride)

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Drug Information of ziprasidone hydrochloride

Product NDC: 55111-257
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: 55111-257
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077565
Marketing Category: ANDA
Start Marketing Date: 20120302

Package Information of ziprasidone hydrochloride

Package NDC: 55111-257-60
Package Description: 60 CAPSULE in 1 BOTTLE (55111-257-60)

NDC Information of ziprasidone hydrochloride

NDC Code 55111-257-60
Proprietary Name ziprasidone hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (55111-257-60)
Product NDC 55111-257
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ziprasidone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120302
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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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