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NDC 51655-0922-52 Isosorbide Mononitrate 30 mg/1 Details

Isosorbide Mononitrate 30 mg/1

Isosorbide Mononitrate is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is ISOSORBIDE MONONITRATE.

MedlinePlus Drug Summary

Isosorbide immediate-release tablets are used for the management of angina (chest pain) in people who have coronary artery disease (narrowing of the blood vessels that supply blood to the heart). Isosorbide extended-release (long-acting) tablets and extended-release capsules are used for the management of chest pain in people who have coronary artery disease. Isosorbide can only be used to prevent angina; it cannot be used to treat an episode of angina once it has begun. Isosorbide is in a class of medications called vasodilators. It works by relaxing the blood vessels so the heart does not need to work as hard and therefore does not need as much oxygen.

Related Packages: 51655-0922-52
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Isosorbide

Product Information

NDC	51655-0922
Product ID	51655-922_0ccd2ec8-bc18-9709-e063-6294a90a3a9d
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Isosorbide Mononitrate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Isosorbide Mononitrate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	30
Active Ingredient Units	mg/1
Substance Name	ISOSORBIDE MONONITRATE
Labeler Name	Northwind Pharmaceuticals, LLC
Pharmaceutical Class	Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA210918
Listing Certified Through	2024-12-31

Package

NDC 51655-0922-52 (51655092252)

Pricing Information	N/A
NDC Package Code	51655-922-52
Billing NDC	51655092252
Package	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-922-52)
Marketing Start Date	2022-03-18
NDC Exclude Flag	N