Isosorbide dinitrate
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Isosorbide dinitrate
- Generic name
- ISOSORBIDE DINITRATE
- Manufacturer
- Northstar Rx LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 246c749d-aa28-44ce-8d42-984660afff2a
- SPL ID
- be0de7ff-f8d9-472f-a35c-252a2cf16954
- Version
- 5
- Effective date
- 2025-08-21
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:32
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 213057 | derived:openfda.application_number |
| application number | ANDA213057 | openfda.application_number | |
| brand name | Isosorbide dinitrate | openfda.brand_name | |
| generic name | ISOSORBIDE DINITRATE | openfda.generic_name | |
| manufacturer name | Northstar Rx LLC | openfda.manufacturer_name | |
| ndc | package | 16714-010-01 | openfda.package_ndc |
| ndc | package | 16714-007-01 | openfda.package_ndc |
| ndc | package | 16714-008-01 | openfda.package_ndc |
| ndc | package | 16714-009-01 | openfda.package_ndc |
| ndc | product | 16714-008 | openfda.product_ndc |
| ndc | product | 16714-007 | openfda.product_ndc |
| ndc | product | 16714-010 | openfda.product_ndc |
| ndc | product | 16714-009 | openfda.product_ndc |
| ndc11 | package | 16714000801 | derived:openfda.package_ndc |
| ndc11 | package | 16714000701 | derived:openfda.package_ndc |
| ndc11 | package | 16714001001 | derived:openfda.package_ndc |
| ndc11 | package | 16714000901 | derived:openfda.package_ndc |
| rxcui | 197839 | openfda.rxcui | |
| rxcui | 314055 | openfda.rxcui | |
| rxcui | 381056 | openfda.rxcui | |
| rxcui | 206842 | openfda.rxcui | |
| spl id | be0de7ff-f8d9-472f-a35c-252a2cf16954 | id | |
| spl set id | 246c749d-aa28-44ce-8d42-984660afff2a | set_id | |
| unii | IA7306519N | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Amplification of the vasodilatory effects of isosorbide dinitrate by sildenafil can result in severe hypotension. The time course and dose dependence of this interaction have not been studied. Appropriate supportive care has not been studied, but it seems reasonable to treat this as a nitrate overdose, with elevation of the extremities and with central volume expansion. The benefits of immediate-release oral isosorbide dinitrate in patients with acute myocardial infarction or congestive heart failure have not been established. If one elects to use isosorbide dinitrate in these conditions, careful clinical or hemodynamic monitoring must be used to avoid the hazards of hypotension and tachycardia. Because the effects of oral isosorbide dinitrate are so difficult to terminate rapidly, this formulation is not recommended in these settings.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Adverse reactions to isosorbide dinitrate are generally dose-related, and almost all of these reactions are the result of isosorbide dinitrate's activity as a vasodilator. Headache, which may be severe, is the most commonly reported side effect. Headache may be recurrent with each daily dose, especially at higher doses. Transient episodes of lightheadedness, occasionally related to blood pressure changes, may also occur. Hypotension occurs infrequently, but in some patients it may be severe enough to warrant discontinuation of therapy. Syncope, crescendo angina, and rebound hypertension have been reported but are uncommon. Extremely rarely, ordinary doses of organic nitrates have caused methemoglobinemia in normal-seeming patients. Methemoglobinemia is so infrequent at these doses that further discussion of its diagnosis and treatment is deferred (see OVERDOSAGE ). Data are not available to allow estimation of the frequency of adverse reactions during treatment with isosorbide dinitrate tablets. To report SUSPECTED ADVERSE REACTIONS, contact NorthStar RxLLC at 1-800-206-7821 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.