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Metoprolol Tartrate - 55154-7460-5 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 55154-7460
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: 55154-7460
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077761
Marketing Category: ANDA
Start Marketing Date: 20070530

Package Information of Metoprolol Tartrate

Package NDC: 55154-7460-5
Package Description: 5 VIAL in 1 BAG (55154-7460-5) > 5 mL in 1 VIAL

NDC Information of Metoprolol Tartrate

NDC Code 55154-7460-5
Proprietary Name Metoprolol Tartrate
Package Description 5 VIAL in 1 BAG (55154-7460-5) > 5 mL in 1 VIAL
Product NDC 55154-7460
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070530
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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