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Haloperidol Decanoate - 63323-469-01 - (HALOPERIDOL DECANOATE)

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Drug Information of Haloperidol Decanoate

Product NDC: 63323-469
Proprietary Name: Haloperidol Decanoate
Non Proprietary Name: HALOPERIDOL DECANOATE
Active Ingredient(s): 50    mg/mL & nbsp;   HALOPERIDOL DECANOATE
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Haloperidol Decanoate

Product NDC: 63323-469
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074893
Marketing Category: ANDA
Start Marketing Date: 20000216

Package Information of Haloperidol Decanoate

Package NDC: 63323-469-01
Package Description: 1 VIAL in 1 CARTON (63323-469-01) > 1 mL in 1 VIAL

NDC Information of Haloperidol Decanoate

NDC Code 63323-469-01
Proprietary Name Haloperidol Decanoate
Package Description 1 VIAL in 1 CARTON (63323-469-01) > 1 mL in 1 VIAL
Product NDC 63323-469
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HALOPERIDOL DECANOATE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 20000216
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name HALOPERIDOL DECANOATE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol Decanoate


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