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Haloperidol - 76237-260-30 - (haloperidol)

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Drug Information of Haloperidol

Product NDC: 76237-260
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: 76237-260
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 20130410

Package Information of Haloperidol

Package NDC: 76237-260-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-260-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Haloperidol

NDC Code 76237-260-30
Proprietary Name Haloperidol
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-260-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130410
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name HALOPERIDOL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


General Information