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Haloperidol - 0615-2595-39 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 0615-2595
Proprietary Name: Haloperidol
Non Proprietary Name: Haloperidol
Active Ingredient(s): 1    mg/1 & nbsp;   Haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 0615-2595
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 20110113

Package Information of Haloperidol

Package NDC: 0615-2595-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-2595-39)

NDC Information of Haloperidol

NDC Code 0615-2595-39
Proprietary Name Haloperidol
Package Description 30 TABLET in 1 BLISTER PACK (0615-2595-39)
Product NDC 0615-2595
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110113
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name HALOPERIDOL
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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