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isosorbide mononitrate - 24236-234-02 - (isosorbide mononitrate)

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Drug Information of isosorbide mononitrate

Product NDC: 24236-234
Proprietary Name: isosorbide mononitrate
Non Proprietary Name: isosorbide mononitrate
Active Ingredient(s): 30    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: 24236-234
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075155
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of isosorbide mononitrate

Package NDC: 24236-234-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (24236-234-02)

NDC Information of isosorbide mononitrate

NDC Code 24236-234-02
Proprietary Name isosorbide mononitrate
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (24236-234-02)
Product NDC 24236-234
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide mononitrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ISOSORBIDE MONONITRATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of isosorbide mononitrate


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