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Haloperidol - 68084-250-21 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 68084-250
Proprietary Name: Haloperidol
Non Proprietary Name: Haloperidol
Active Ingredient(s): 20    mg/1 & nbsp;   Haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 68084-250
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077580
Marketing Category: ANDA
Start Marketing Date: 20080402

Package Information of Haloperidol

Package NDC: 68084-250-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-250-21) > 10 TABLET in 1 BLISTER PACK (68084-250-01)

NDC Information of Haloperidol

NDC Code 68084-250-21
Proprietary Name Haloperidol
Package Description 3 BLISTER PACK in 1 CARTON (68084-250-21) > 10 TABLET in 1 BLISTER PACK (68084-250-01)
Product NDC 68084-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080402
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name HALOPERIDOL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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