Isosorbide Mononitrate (Ingenus Pharmaceuticals, LLC): FDA Package Insert, Page... (2024)

Ingenus Pharmaceuticals, LLC

Methemoglobinemia

Methemoglobinemia has been reported in patients receiving other organic nitrates, and it probably could also occur as a side effect of isosorbide mononitrate. Certainly nitrate ions liberated during metabolism of isosorbide mononitrate can oxidize hemoglobin into methemoglobin. Even in patients totally without cytochrome b5 reductase activity, however, and even assuming that the nitrate moiety of isosorbide mononitrate is quantitatively applied to oxidation of hemoglobin, about 2 mg/kg of isosorbide mononitrate should be required before any of these patients manifest clinically significant (≥10%) methemoglobinemia. In patients with normal reductase function, significant production of methemoglobin should require even larger doses of isosorbide mononitrate. In one study in which 36 patients received 2 to 4 weeks of continuous nitroglycerin therapy at 3.1 to 4.4 mg/hr (equivalent, in total administered dose of nitrate ions, to 7.8 to 11.1 mg of isosorbide mononitrate per hour), the average methemoglobin level measured was 0.2%; this was comparable to that observed in parallel patients who received placebo.

Not with standing these observations, there are case reports of significant methemoglobinemia in association with moderate overdoses of organic nitrates. None of the affected patients had been thought to be unusually susceptible.

Methemoglobin levels are available from most clinical laboratories. The diagnosis should be suspected in patients who exhibit signs of impaired oxygen delivery despite adequate cardiac output and adequate arterial pO2 . Classically, methemoglobinemic blood is described as chocolate brown without color change on exposure to air. When methemoglobinemia is diagnosed, the treatment of choice is methylene blue, 1 to 2 mg/kg intravenously.

DOSAGE AND ADMINISTRATION

The recommended starting dose of Isosorbide Mononitrate Extended-Release Tablets, USP is 30 mg (given as a single 30 mg tablet or as 1/2 of a 60 mg tablet) or 60 mg (given as a single tablet) once daily. After several days, the dosage may be increased to 120 mg (given as a single 120 mg tablet or as two 60 mg tablets) once daily. Rarely, 240 mg may be required. The daily dose of Isosorbide Mononitrate Extended-Release Tablets, USP should be taken in the morning on arising. Isosorbide Mononitrate Extended-Release Tablets, USP should not be chewed or crushed and should be swallowed together with a half-glassful of fluid.

HOW SUPPLIED

Isosorbide Mononitrate Extended-Release Tablets USP, 30 mg are white to off-white, uncoated, oval shaped tablets debossed with ‘ING 175’ one side and scored on the other side. They are supplied as follows:

Bottles of 100 NDC 50742-175-01

Bottles of 500 NDC 50742-175-05

Isosorbide Mononitrate Extended-Release Tablets USP, 60 mg are white to off-white, uncoated, capsule shaped tablets debossed with ‘ING 176’ one side and scored on the other side. They are supplied as follows:

Bottles of 100 NDC 50742-176-01

Bottles of 500 NDC 50742-176-05

Isosorbide Mononitrate Extended-Release Tablets USP, 120 mg are white to off-white, uncoated, oval shaped tablets debossed with ‘ING 177’ one side and plain on the other side. They are supplied as follows:

Bottles of 100 NDC 50742-177-01

Store at 20o -30o C (68o -86o F) [See USP Controlled Room Temperature].

Manufactured for:

Ingenus Pharmaceuticals, LLC

Orlando, FL 32811-7193

Made in India

DRUGS/TS/23/2007

Rev.: 09/2023

Isosorbide Mononitrate (Ingenus Pharmaceuticals, LLC): FDA Package Insert, Page... (1)Ingenus Logo

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label — Principal Display Panel – 30 mg, 100 Tablets

ingenus

NDC 50742-175-01

Isosorbide Mononitrate Extended-Release Tablets, USP

30 mg

Rx Only

100 Tablets

(click image for full-size original)

30 mg Tablet -100s Count Bottle Label

Package Label — Principal Display Panel – 30 mg, 500 Tablets

ingenus

NDC 50742-175-05

Isosorbide Mononitrate Extended-Release Tablets, USP

30 mg

Rx Only

500 Tablets

(click image for full-size original)

30 mg Tablet -500s Count Bottle Label

Package Label — Principal Display Panel – 60 mg, 100 Tablets

ingenus

NDC 50742-176-01

Isosorbide Mononitrate Extended-Release Tablets, USP

60 mg

Rx Only

100 Tablets

(click image for full-size original)

60 mg Tablet -100s Count Bottle Label

Package Label — Principal Display Panel – 60 mg, 500 Tablets

ingenus

NDC 50742-176-05

Isosorbide Mononitrate Extended-Release Tablets, USP

60 mg

Rx Only

500 Tablets

(click image for full-size original)

60 mg Tablet -500s Count Bottle Label

Package Label — Principal Display Panel – 120 mg, 100 Tablets

ingenus

NDC 50742-177-01

Isosorbide Mononitrate Extended-Release Tablets, USP

120 mg

Rx Only

100 Tablets

(click image for full-size original)

120 mg Tablet -100s Count Bottle Label

ISOSORBIDE MONONITRATE isosorbide mononitrate tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50742-175
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOSORBIDE MONONITRATE (ISOSORBIDE MONONITRATE) ISOSORBIDE MONONITRATE 30 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
HYDROXYPROPYL CELLULOSE (1200000 WAMW)
HYPROMELLOSE 2208 (100000 MPA.S)
SILICON DIOXIDE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape OVAL Size 9mm
Flavor Imprint Code ING175
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50742-175-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC None
2 NDC:50742-175-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA210918 11/13/2018
ISOSORBIDE MONONITRATE isosorbide mononitrate tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50742-176
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOSORBIDE MONONITRATE (ISOSORBIDE MONONITRATE) ISOSORBIDE MONONITRATE 60 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSE 2208 (100000 MPA.S)
SILICON DIOXIDE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (1200000 WAMW)
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape CAPSULE Size 14mm
Flavor Imprint Code ING176
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50742-176-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC None
2 NDC:50742-176-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA210918 11/13/2018
ISOSORBIDE MONONITRATE isosorbide mononitrate tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50742-177
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOSORBIDE MONONITRATE (ISOSORBIDE MONONITRATE) ISOSORBIDE MONONITRATE 120 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSE 2208 (100000 MPA.S)
SILICON DIOXIDE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (1200000 WAMW)
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape OVAL Size 16mm
Flavor Imprint Code ING177
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50742-177-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA210918 11/13/2018

Labeler — Ingenus Pharmaceuticals, LLC (833250017)

Registrant — RICONPHARMA LLC (859035318)

Establishment
Name Address ID/FEI Operations
COHANCE LIFESCIENCES LIMITED 677637710 MANUFACTURE (50742-175), MANUFACTURE (50742-176), MANUFACTURE (50742-177)

Revised: 10/2023 Ingenus Pharmaceuticals, LLC

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

https://medlibrary.org/lib/rx/meds/isosorbide-mononitrate-30/page/4/

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