Isosorbide Mononitrate NDC 50742-177

Product information

Brand name (proprietary)

Isosorbide Mononitrate

Generic name (nonproprietary)

isosorbide mononitrate

Active ingredients

Isosorbide mononitrate — 120 mg/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

Ingenus Pharmaceuticals, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 210918

Marketing start

Nov 13, 2018

Listing expires

Dec 31, 2026

Other FDA classes

Nitrates (Chemical structure)Vasodilation (Physiologic effect)

Identifiers

Product ID 50742-177_1548dff4-f987-4dbe-87ec-f4e9d1d60366SPL ID 1548dff4-f987-4dbe-87ec-f4e9d1d60366SPL set ID c950760f-0e32-483f-96f2-eecaf057c0ecRxCUI 311196, 317110, 353538UNII LX1OH63030UPC 0350742176014, 0350742175017, 0350742176052, 0350742175055, 0350742177011

Pharmacologic class

Nitrate Vasodilator

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450742017701 followed by a unit qualifier and the quantity Copy

Package 50742-0177-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 210918

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.