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Haloperidol - 54868-2570-2 - (haloperidol)

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Drug Information of Haloperidol

Product NDC: 54868-2570
Proprietary Name: Haloperidol
Non Proprietary Name: haloperidol
Active Ingredient(s): .5    mg/1 & nbsp;   haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 54868-2570
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 19990429

Package Information of Haloperidol

Package NDC: 54868-2570-2
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-2570-2)

NDC Information of Haloperidol

NDC Code 54868-2570-2
Proprietary Name Haloperidol
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-2570-2)
Product NDC 54868-2570
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990429
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HALOPERIDOL
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


General Information