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Labetalol hydrochloride - 0591-0606-10 - (Labetalol hydrochloride)

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Drug Information of Labetalol hydrochloride

Product NDC: 0591-0606
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: 0591-0606
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075133
Marketing Category: ANDA
Start Marketing Date: 19980803

Package Information of Labetalol hydrochloride

Package NDC: 0591-0606-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-10)

NDC Information of Labetalol hydrochloride

NDC Code 0591-0606-10
Proprietary Name Labetalol hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-10)
Product NDC 0591-0606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980803
Marketing Category Name ANDA
Labeler Name Watson 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 hydrochloride


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