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Haloperidol - 63323-474-01 - (HALOPERIDOL LACTATE)

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Drug Information of Haloperidol

Product NDC: 63323-474
Proprietary Name: Haloperidol
Non Proprietary Name: HALOPERIDOL LACTATE
Active Ingredient(s): 5    mg/mL & nbsp;   HALOPERIDOL LACTATE
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol

Product NDC: 63323-474
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075689
Marketing Category: ANDA
Start Marketing Date: 20110328

Package Information of Haloperidol

Package NDC: 63323-474-01
Package Description: 25 VIAL in 1 TRAY (63323-474-01) > 1 mL in 1 VIAL

NDC Information of Haloperidol

NDC Code 63323-474-01
Proprietary Name Haloperidol
Package Description 25 VIAL in 1 TRAY (63323-474-01) > 1 mL in 1 VIAL
Product NDC 63323-474
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HALOPERIDOL LACTATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20110328
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name HALOPERIDOL LACTATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol


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