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Haloperidol - 51079-733-20 - (haloperidol)

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Drug Information of Haloperidol

Product NDC: 51079-733
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: 51079-733
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 20120925

Package Information of Haloperidol

Package NDC: 51079-733-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-733-20) > 1 TABLET in 1 BLISTER PACK (51079-733-01)

NDC Information of Haloperidol

NDC Code 51079-733-20
Proprietary Name Haloperidol
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-733-20) > 1 TABLET in 1 BLISTER PACK (51079-733-01)
Product NDC 51079-733
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120925
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name HALOPERIDOL
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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