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Haloperidol - 0781-1397-10 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 0781-1397
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: 0781-1397
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071210
Marketing Category: ANDA
Start Marketing Date: 19880311

Package Information of Haloperidol

Package NDC: 0781-1397-10
Package Description: 1000 TABLET in 1 BOTTLE (0781-1397-10)

NDC Information of Haloperidol

NDC Code 0781-1397-10
Proprietary Name Haloperidol
Package Description 1000 TABLET in 1 BOTTLE (0781-1397-10)
Product NDC 0781-1397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880311
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name HALOPERIDOL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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