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Haloperidol Lactate - 25021-806-01 - (haloperidol lactate)

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Drug Information of Haloperidol Lactate

Product NDC: 25021-806
Proprietary Name: Haloperidol Lactate
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 Lactate

Product NDC: 25021-806
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091637
Marketing Category: ANDA
Start Marketing Date: 20111024

Package Information of Haloperidol Lactate

Package NDC: 25021-806-01
Package Description: 10 VIAL in 1 CARTON (25021-806-01) > 1 mL in 1 VIAL

NDC Information of Haloperidol Lactate

NDC Code 25021-806-01
Proprietary Name Haloperidol Lactate
Package Description 10 VIAL in 1 CARTON (25021-806-01) > 1 mL in 1 VIAL
Product NDC 25021-806
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name haloperidol lactate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20111024
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name HALOPERIDOL LACTATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol Lactate


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