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Haloperidol Decanoate - 0703-7021-03 - (Haloperidol Decanoate)

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Drug Information of Haloperidol Decanoate

Product NDC: 0703-7021
Proprietary Name: Haloperidol Decanoate
Non Proprietary Name: Haloperidol Decanoate
Active Ingredient(s): 100    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: 0703-7021
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075393
Marketing Category: ANDA
Start Marketing Date: 19990604

Package Information of Haloperidol Decanoate

Package NDC: 0703-7021-03
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7021-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7021-01)

NDC Information of Haloperidol Decanoate

NDC Code 0703-7021-03
Proprietary Name Haloperidol Decanoate
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7021-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7021-01)
Product NDC 0703-7021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haloperidol Decanoate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 19990604
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name HALOPERIDOL DECANOATE
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Haloperidol Decanoate


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