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LABETALOL HYDROCHLORIDE - 16590-994-60 - (LABETALOL HYDROCHLORIDE)

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Drug Information of LABETALOL HYDROCHLORIDE

Product NDC: 16590-994
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: 16590-994
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075133
Marketing Category: ANDA
Start Marketing Date: 19980803

Package Information of LABETALOL HYDROCHLORIDE

Package NDC: 16590-994-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (16590-994-60)

NDC Information of LABETALOL HYDROCHLORIDE

NDC Code 16590-994-60
Proprietary Name LABETALOL HYDROCHLORIDE
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (16590-994-60)
Product NDC 16590-994
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 STAT RX USA LLC
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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