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Metoprolol Tartrate - 49999-226-60 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 49999-226
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol Tartrate
Active Ingredient(s): 100    mg/1 & nbsp;   Metoprolol Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 49999-226
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078459
Marketing Category: ANDA
Start Marketing Date: 20120316

Package Information of Metoprolol Tartrate

Package NDC: 49999-226-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (49999-226-60)

NDC Information of Metoprolol Tartrate

NDC Code 49999-226-60
Proprietary Name Metoprolol Tartrate
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (49999-226-60)
Product NDC 49999-226
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120316
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name METOPROLOL TARTRATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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