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Metoprolol Tartrate - 68788-9890-3 - (Metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 68788-9890
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: 68788-9890
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 20120214

Package Information of Metoprolol Tartrate

Package NDC: 68788-9890-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9890-3)

NDC Information of Metoprolol Tartrate

NDC Code 68788-9890-3
Proprietary Name Metoprolol Tartrate
Package Description 30 TABLET in 1 BOTTLE (68788-9890-3)
Product NDC 68788-9890
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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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