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Metoprolol Tartrate - 0517-1355-25 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0517-1355
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol Tartrate
Active Ingredient(s): 1    mg/mL & nbsp;   Metoprolol Tartrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 0517-1355
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090386
Marketing Category: ANDA
Start Marketing Date: 20100211

Package Information of Metoprolol Tartrate

Package NDC: 0517-1355-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-1355-25) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Metoprolol Tartrate

NDC Code 0517-1355-25
Proprietary Name Metoprolol Tartrate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-1355-25) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-1355
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100211
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name METOPROLOL TARTRATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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