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Nitroglycerin - 0517-4810-25 - (nitroglycerin)

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Drug Information of Nitroglycerin

Product NDC: 0517-4810
Proprietary Name: Nitroglycerin
Non Proprietary Name: nitroglycerin
Active Ingredient(s): 5    mg/mL & nbsp;   nitroglycerin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nitroglycerin

Product NDC: 0517-4810
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072034
Marketing Category: ANDA
Start Marketing Date: 20030304

Package Information of Nitroglycerin

Package NDC: 0517-4810-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4810-25) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Nitroglycerin

NDC Code 0517-4810-25
Proprietary Name Nitroglycerin
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4810-25) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-4810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nitroglycerin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030304
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name NITROGLYCERIN
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Nitroglycerin


General Information