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Labetalol Hydrochloride - 54868-4903-0 - (Labetalol Hydrochloride)

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Drug Information of Labetalol Hydrochloride

Product NDC: 54868-4903
Proprietary Name: Labetalol Hydrochloride
Non Proprietary Name: Labetalol Hydrochloride
Active Ingredient(s): 300    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: 54868-4903
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074787
Marketing Category: ANDA
Start Marketing Date: 20040825

Package Information of Labetalol Hydrochloride

Package NDC: 54868-4903-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4903-0)

NDC Information of Labetalol Hydrochloride

NDC Code 54868-4903-0
Proprietary Name Labetalol Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4903-0)
Product NDC 54868-4903
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040825
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LABETALOL HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Labetalol Hydrochloride


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