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Labetalol HCl - 63739-366-10 - (Labetalol HCl)

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Drug Information of Labetalol HCl

Product NDC: 63739-366
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: 63739-366
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075113
Marketing Category: ANDA
Start Marketing Date: 20061115

Package Information of Labetalol HCl

Package NDC: 63739-366-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-366-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Labetalol HCl

NDC Code 63739-366-10
Proprietary Name Labetalol HCl
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-366-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-366
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061115
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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