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Metoprolol Tartrate - 52584-285-05 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 52584-285
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: 52584-285
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075160
Marketing Category: ANDA
Start Marketing Date: 20100801

Package Information of Metoprolol Tartrate

Package NDC: 52584-285-05
Package Description: 1 AMPULE in 1 BAG (52584-285-05) > 5 mL in 1 AMPULE

NDC Information of Metoprolol Tartrate

NDC Code 52584-285-05
Proprietary Name Metoprolol Tartrate
Package Description 1 AMPULE in 1 BAG (52584-285-05) > 5 mL in 1 AMPULE
Product NDC 52584-285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100801
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, 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


General Information