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Metoprolol Tartrate - 55390-073-10 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 55390-073
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol Tartrate
Active Ingredient(s): 5    mg/5mL & 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: 55390-073
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076495
Marketing Category: ANDA
Start Marketing Date: 20030717

Package Information of Metoprolol Tartrate

Package NDC: 55390-073-10
Package Description: 10 VIAL in 1 BOX (55390-073-10) > 5 mL in 1 VIAL

NDC Information of Metoprolol Tartrate

NDC Code 55390-073-10
Proprietary Name Metoprolol Tartrate
Package Description 10 VIAL in 1 BOX (55390-073-10) > 5 mL in 1 VIAL
Product NDC 55390-073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030717
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name METOPROLOL TARTRATE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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