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HALOPERIDOL - 24236-652-02 - (HALOPERIDOL)

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Drug Information of HALOPERIDOL

Product NDC: 24236-652
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: 24236-652
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071208
Marketing Category: ANDA
Start Marketing Date: 20101220

Package Information of HALOPERIDOL

Package NDC: 24236-652-02
Package Description: 30 TABLET in 1 BLISTER PACK (24236-652-02)

NDC Information of HALOPERIDOL

NDC Code 24236-652-02
Proprietary Name HALOPERIDOL
Package Description 30 TABLET in 1 BLISTER PACK (24236-652-02)
Product NDC 24236-652
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HALOPERIDOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101220
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HALOPERIDOL
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of HALOPERIDOL


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