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Labetalol Hydrochloride - 17478-420-20 - (Labetalol Hydrochloride)

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Drug Information of Labetalol Hydrochloride

Product NDC: 17478-420
Proprietary Name: Labetalol Hydrochloride
Non Proprietary Name: Labetalol Hydrochloride
Active Ingredient(s): 5    mg/mL & nbsp;   Labetalol Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Labetalol Hydrochloride

Product NDC: 17478-420
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075431
Marketing Category: ANDA
Start Marketing Date: 20040901

Package Information of Labetalol Hydrochloride

Package NDC: 17478-420-20
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (17478-420-20) > 20 mL in 1 VIAL, MULTI-DOSE

NDC Information of Labetalol Hydrochloride

NDC Code 17478-420-20
Proprietary Name Labetalol Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (17478-420-20) > 20 mL in 1 VIAL, MULTI-DOSE
Product NDC 17478-420
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20040901
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name LABETALOL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Labetalol Hydrochloride


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