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Labetalol hydrochloride - 0904-5929-61 - (Labetalol hydrochloride)

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Drug Information of Labetalol hydrochloride

Product NDC: 0904-5929
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
Coding System: National Drug Codes(NDC)

Labeler Information of Labetalol hydrochloride

Product NDC: 0904-5929
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075133
Marketing Category: ANDA
Start Marketing Date: 20090610

Package Information of Labetalol hydrochloride

Package NDC: 0904-5929-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5929-61)

NDC Information of Labetalol hydrochloride

NDC Code 0904-5929-61
Proprietary Name Labetalol hydrochloride
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5929-61)
Product NDC 0904-5929
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Labetalol hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090610
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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