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Haloperidol - 55154-6272-9 - (haloperidol)

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Drug Information of Haloperidol

Product NDC: 55154-6272
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: 55154-6272
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 20120905

Package Information of Haloperidol

Package NDC: 55154-6272-9
Package Description: 30 TABLET in 1 BLISTER PACK (55154-6272-9)

NDC Information of Haloperidol

NDC Code 55154-6272-9
Proprietary Name Haloperidol
Package Description 30 TABLET in 1 BLISTER PACK (55154-6272-9)
Product NDC 55154-6272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120905
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name HALOPERIDOL
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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