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Nitroglycerin - 21695-810-00 - (Nitroglycerin)

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Drug Information of Nitroglycerin

Product NDC: 21695-810
Proprietary Name: Nitroglycerin
Non Proprietary Name: Nitroglycerin
Active Ingredient(s): .4    mg/1 & nbsp;   Nitroglycerin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nitroglycerin

Product NDC: 21695-810
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050303

Package Information of Nitroglycerin

Package NDC: 21695-810-00
Package Description: 100 TABLET in 1 BOTTLE (21695-810-00)

NDC Information of Nitroglycerin

NDC Code 21695-810-00
Proprietary Name Nitroglycerin
Package Description 100 TABLET in 1 BOTTLE (21695-810-00)
Product NDC 21695-810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitroglycerin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050303
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Rebel Distributors Corp
Substance Name NITROGLYCERIN
Strength Number .4
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Nitroglycerin


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