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Haloperidol - 68382-080-10 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 68382-080
Proprietary Name: Haloperidol
Non Proprietary Name: Haloperidol
Active Ingredient(s): 10    mg/1 & nbsp;   Haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 68382-080
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077580
Marketing Category: ANDA
Start Marketing Date: 20080103

Package Information of Haloperidol

Package NDC: 68382-080-10
Package Description: 1000 TABLET in 1 BOTTLE (68382-080-10)

NDC Information of Haloperidol

NDC Code 68382-080-10
Proprietary Name Haloperidol
Package Description 1000 TABLET in 1 BOTTLE (68382-080-10)
Product NDC 68382-080
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080103
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name HALOPERIDOL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


General Information