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Labetalol HCl - 51079-929-20 - (Labetalol HCl)

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Drug Information of Labetalol HCl

Product NDC: 51079-929
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: 51079-929
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075113
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Labetalol HCl

Package NDC: 51079-929-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-929-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-929-01)

NDC Information of Labetalol HCl

NDC Code 51079-929-20
Proprietary Name Labetalol HCl
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-929-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-929-01)
Product NDC 51079-929
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 UDL Laboratories, 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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