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Haloperidol - 21695-653-60 - (Haloperidol)

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Drug Information of Haloperidol

Product NDC: 21695-653
Proprietary Name: Haloperidol
Non Proprietary Name: Haloperidol
Active Ingredient(s): 5    mg/1 & nbsp;   Haloperidol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 21695-653
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071209
Marketing Category: ANDA
Start Marketing Date: 19861117

Package Information of Haloperidol

Package NDC: 21695-653-60
Package Description: 60 TABLET in 1 BOTTLE (21695-653-60)

NDC Information of Haloperidol

NDC Code 21695-653-60
Proprietary Name Haloperidol
Package Description 60 TABLET in 1 BOTTLE (21695-653-60)
Product NDC 21695-653
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861117
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HALOPERIDOL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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