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METOPROLOL TARTRATE - 54868-5726-0 - (metoprolol tartrate)

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Drug Information of METOPROLOL TARTRATE

Product NDC: 54868-5726
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: 54868-5726
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076495
Marketing Category: ANDA
Start Marketing Date: 20061211

Package Information of METOPROLOL TARTRATE

Package NDC: 54868-5726-0
Package Description: 10 VIAL in 1 BOX (54868-5726-0) > 5 mL in 1 VIAL

NDC Information of METOPROLOL TARTRATE

NDC Code 54868-5726-0
Proprietary Name METOPROLOL TARTRATE
Package Description 10 VIAL in 1 BOX (54868-5726-0) > 5 mL in 1 VIAL
Product NDC 54868-5726
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20061211
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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