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Metoprolol Tartrate - 0409-2285-05 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0409-2285
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol Tartrate
Active Ingredient(s): 1    mg/mL & 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: 0409-2285
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075160
Marketing Category: ANDA
Start Marketing Date: 19980706

Package Information of Metoprolol Tartrate

Package NDC: 0409-2285-05
Package Description: 3 AMPULE in 1 CARTON (0409-2285-05) > 5 mL in 1 AMPULE

NDC Information of Metoprolol Tartrate

NDC Code 0409-2285-05
Proprietary Name Metoprolol Tartrate
Package Description 3 AMPULE in 1 CARTON (0409-2285-05) > 5 mL in 1 AMPULE
Product NDC 0409-2285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19980706
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name METOPROLOL TARTRATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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