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Haloperidol - 0378-0214-10 - (haloperidol)

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Drug Information of Haloperidol

Product NDC: 0378-0214
Proprietary Name: Haloperidol
Non Proprietary Name: haloperidol
Active Ingredient(s): 2    mg/1 & nbsp;   haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 0378-0214
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070278
Marketing Category: ANDA
Start Marketing Date: 20120905

Package Information of Haloperidol

Package NDC: 0378-0214-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0214-10)

NDC Information of Haloperidol

NDC Code 0378-0214-10
Proprietary Name Haloperidol
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0214-10)
Product NDC 0378-0214
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 Mylan Pharmaceuticals Inc.
Substance Name HALOPERIDOL
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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