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Labetalol HCl - 0185-0117-10 - (Labetalol HCl)

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Drug Information of Labetalol HCl

Product NDC: 0185-0117
Proprietary Name: Labetalol HCl
Non Proprietary Name: Labetalol HCl
Active Ingredient(s): 200    mg/1 & nbsp;   Labetalol HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Labetalol HCl

Product NDC: 0185-0117
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075113
Marketing Category: ANDA
Start Marketing Date: 19980804

Package Information of Labetalol HCl

Package NDC: 0185-0117-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0185-0117-10)

NDC Information of Labetalol HCl

NDC Code 0185-0117-10
Proprietary Name Labetalol HCl
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0185-0117-10)
Product NDC 0185-0117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980804
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name LABETALOL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Labetalol HCl


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