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Labetalol HCl - 55154-5491-0 - (Labetalol HCl)

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Drug Information of Labetalol HCl

Product NDC: 55154-5491
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: 55154-5491
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075113
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Labetalol HCl

Package NDC: 55154-5491-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5491-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Labetalol HCl

NDC Code 55154-5491-0
Proprietary Name Labetalol HCl
Package Description 10 BLISTER PACK in 1 BAG (55154-5491-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110506
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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