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Isosorbide Mononitrate - 0615-7757-05 - (Isosorbide Mononitrate)

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Drug Information of Isosorbide Mononitrate

Product NDC: 0615-7757
Proprietary Name: Isosorbide Mononitrate
Non Proprietary Name: Isosorbide Mononitrate
Active Ingredient(s): 60    mg/1 & nbsp;   Isosorbide Mononitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide Mononitrate

Product NDC: 0615-7757
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090598
Marketing Category: ANDA
Start Marketing Date: 20100811

Package Information of Isosorbide Mononitrate

Package NDC: 0615-7757-05
Package Description: 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7757-05)

NDC Information of Isosorbide Mononitrate

NDC Code 0615-7757-05
Proprietary Name Isosorbide Mononitrate
Package Description 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7757-05)
Product NDC 0615-7757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Mononitrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100811
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name ISOSORBIDE MONONITRATE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Isosorbide Mononitrate


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