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Labetalol hydrochloride - 68084-456-01 - (Labetalol hydrochloride)

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Drug Information of Labetalol hydrochloride

Product NDC: 68084-456
Proprietary Name: Labetalol hydrochloride
Non Proprietary Name: Labetalol hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Labetalol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Labetalol hydrochloride

Product NDC: 68084-456
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075133
Marketing Category: ANDA
Start Marketing Date: 20110211

Package Information of Labetalol hydrochloride

Package NDC: 68084-456-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-456-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-456-11)

NDC Information of Labetalol hydrochloride

NDC Code 68084-456-01
Proprietary Name Labetalol hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-456-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-456-11)
Product NDC 68084-456
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110211
Marketing Category Name ANDA
Labeler Name American Health Packaging
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 hydrochloride


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