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Haloperidol - 54838-501-40 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 54838-501
Proprietary Name: Haloperidol
Non Proprietary Name: Haloperidol
Active Ingredient(s): 2    mg/mL & nbsp;   Haloperidol
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 54838-501
Labeler Name: Silarx Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073364
Marketing Category: ANDA
Start Marketing Date: 20090908

Package Information of Haloperidol

Package NDC: 54838-501-40
Package Description: 120 mL in 1 BOTTLE, DROPPER (54838-501-40)

NDC Information of Haloperidol

NDC Code 54838-501-40
Proprietary Name Haloperidol
Package Description 120 mL in 1 BOTTLE, DROPPER (54838-501-40)
Product NDC 54838-501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20090908
Marketing Category Name ANDA
Labeler Name Silarx Pharmaceuticals, Inc
Substance Name HALOPERIDOL LACTATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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