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Metoprolol Tartrate - 51138-107-30 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 51138-107
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol Tartrate
Active Ingredient(s): 50    mg/1 & nbsp;   Metoprolol Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 51138-107
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 20110115

Package Information of Metoprolol Tartrate

Package NDC: 51138-107-30
Package Description: 30 TABLET in 1 BOTTLE (51138-107-30)

NDC Information of Metoprolol Tartrate

NDC Code 51138-107-30
Proprietary Name Metoprolol Tartrate
Package Description 30 TABLET in 1 BOTTLE (51138-107-30)
Product NDC 51138-107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110115
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
Substance Name METOPROLOL TARTRATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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