NITRO-TIME
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
- NITRO-TIME
- Generic name
- NITROGLYCERIN
- Manufacturer
- TIME CAP LABORATORIES, INC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3c11c1c2-8e62-4f63-8293-2f8b8d845f7e
- SPL ID
- 51ed5c69-89ac-27ed-e063-6394a90acca1
- Version
- 8
- Effective date
- 2026-05-18
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:33
| 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 |
|---|---|---|---|
| brand name | NITRO-TIME | openfda.brand_name | |
| generic name | NITROGLYCERIN | openfda.generic_name | |
| manufacturer name | TIME CAP LABORATORIES, INC | openfda.manufacturer_name | |
| ndc | package | 49483-222-06 | openfda.package_ndc |
| ndc | package | 49483-223-06 | openfda.package_ndc |
| ndc | package | 49483-221-06 | openfda.package_ndc |
| ndc | package | 49483-221-10 | openfda.package_ndc |
| ndc | package | 49483-223-10 | openfda.package_ndc |
| ndc | package | 49483-222-10 | openfda.package_ndc |
| ndc | product | 49483-223 | openfda.product_ndc |
| ndc | product | 49483-222 | openfda.product_ndc |
| ndc | product | 49483-221 | openfda.product_ndc |
| ndc11 | package | 49483022206 | derived:openfda.package_ndc |
| ndc11 | package | 49483022110 | derived:openfda.package_ndc |
| ndc11 | package | 49483022210 | derived:openfda.package_ndc |
| ndc11 | package | 49483022310 | derived:openfda.package_ndc |
| ndc11 | package | 49483022306 | derived:openfda.package_ndc |
| ndc11 | package | 49483022106 | derived:openfda.package_ndc |
| rxcui | 312018 | openfda.rxcui | |
| rxcui | 312020 | openfda.rxcui | |
| rxcui | 312013 | openfda.rxcui | |
| spl id | 51ed5c69-89ac-27ed-e063-6394a90acca1 | id | |
| spl set id | 3c11c1c2-8e62-4f63-8293-2f8b8d845f7e | set_id | |
| unii | G59M7S0WS3 | 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 nitroglycerin by phosphodiesterase inhibitors 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 oral nitroglycerin in patients with acute myocardial infarction or congestive heart failure have not been established. If one elects to use nitroglycerin in these conditions, careful clinical or hemodynamic monitoring must be used to avoid the hazards of hypotension and tachycardia. Because the effects at capsules are so difficult to terminate rapidly, that are not recommended in these settings. PRECAUTIONS: General: Severe hypotension, particularly with upright posture, may occur with even small doses of nitroglycerin. This drug should therefore be used with caution in patients who may be volume depleted or who, for whatever reason, are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris. Nitrate therapy may aggravate the angina caused by hypertrophic cardiomyopathy. As tolerance in other forms of nitroglycerin develops, the effect of sublingual nitroglycerin on exercise tolerance, although still observable, is somewhat blunted. In industrial workers who have had long-term exposure to unknown (presumably high) doses of organic nitrates, tolerance clearly occurs. Chest pain, acute myocardial infarction, and even sudden death have occurred during temporary withdrawal of nitrates from these workers, demonstrating the existence of true physical dependence. Some clinical trials in angina patients have provided nitroglycerin for about 12 continuous hours of every 24-hour day. During the nitrate-free intervals in some of these trials, anginal attacks have been more easily provoked than before treatment, and patients have demonstrated hemodynamic rebound and decreased exercise tolerance. The importance of these observations to the routine, clinical use at oral nitroglycerin is not known.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS: Adverse reactions to nitroglycerin are generally dose-related, and almost all of these reactions are the result of nitroglycerin'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 may be severe enough to warrant discontinuation of therapy. Syncope, crescendo angina, and rebound hypertension have been reported but are uncommon. Allergic reactions to nitroglycerin are also uncommon, and the great majority of those reported have been cases of contact dermatitis or fixed drug eruptions in patients receiving nitroglycerin in ointments or patches. There have been a few reports of genuine anaphylactoid reactions, and these reactions can probably occur in patients receiving nitroglycerin by any route. Extremely rarely, ordinary doses of organic nitrates have caused methemoglobinemia in normal seeming patients; for further discussion of its diagnosis and treatment see OVERDOSAGE. Data are not available to allow estimation of the frequency of adverse reactions during treatment with Nitroglycerin Extended-Release Capsules.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.