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Labetalol Hydrochloride - 67457-280-40 - (labetalol)

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Drug Information of Labetalol Hydrochloride

Product NDC: 67457-280
Proprietary Name: Labetalol Hydrochloride
Non Proprietary Name: labetalol
Active Ingredient(s): 5    mg/mL & nbsp;   labetalol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Labetalol Hydrochloride

Product NDC: 67457-280
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090699
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Labetalol Hydrochloride

Package NDC: 67457-280-40
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (67457-280-40) > 40 mL in 1 VIAL, MULTI-DOSE

NDC Information of Labetalol Hydrochloride

NDC Code 67457-280-40
Proprietary Name Labetalol Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (67457-280-40) > 40 mL in 1 VIAL, MULTI-DOSE
Product NDC 67457-280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name labetalol
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name LABETALOL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Labetalol Hydrochloride


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