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Metoprolol Tartrate - 68645-190-59 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 68645-190
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 68645-190
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077739
Marketing Category: ANDA
Start Marketing Date: 20070911

Package Information of Metoprolol Tartrate

Package NDC: 68645-190-59
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (68645-190-59)

NDC Information of Metoprolol Tartrate

NDC Code 68645-190-59
Proprietary Name Metoprolol Tartrate
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (68645-190-59)
Product NDC 68645-190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070911
Marketing Category Name ANDA
Labeler Name Legacy Pharmaceutical Packaging
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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