NITROGLYCERIN
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
- NITROGLYCERIN
- Generic name
- NITROGLYCERIN
- Manufacturer
- Trupharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 543ef8c8-d520-461b-bf6e-f8d8c277feec
- SPL ID
- 28693a60-dc7a-eacb-e063-6394a90ae222
- Version
- 1
- Effective date
- 2024-12-03
- 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 06:24:57
| Harmonized routes |
|---|
| RECTAL |
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 | 212222 | derived:openfda.application_number |
| application number | ANDA212222 | openfda.application_number | |
| brand name | NITROGLYCERIN | openfda.brand_name | |
| generic name | NITROGLYCERIN | openfda.generic_name | |
| manufacturer name | Trupharma, LLC | openfda.manufacturer_name | |
| ndc | package | 52817-835-30 | openfda.package_ndc |
| ndc | product | 52817-835 | openfda.product_ndc |
| ndc11 | package | 52817083530 | derived:openfda.package_ndc |
| rxcui | 1114466 | openfda.rxcui | |
| spl id | 28693a60-dc7a-eacb-e063-6394a90ae222 | id | |
| spl set id | 543ef8c8-d520-461b-bf6e-f8d8c277feec | set_id | |
| unii | G59M7S0WS3 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS Cardiovascular Disorders: Venous and arterial dilatation as a consequence of nitroglycerin treatment can result in hypotension. Exercise caution when treating patients with any of the following conditions: blood volume depletion, existing hypotension, cardiomyopathies, congestive heart failure, acute myocardial infarction, or poor cardiac function for other reasons ( 5.1 ). Headache: Nitroglycerin produces dose-related headaches which may be severe ( 5.2 ) 5.1 Cardiovascular Disorders Venous and arterial dilatation as a consequence of nitroglycerin treatment including nitroglycerin ointment, 0.4%, can decrease venous blood returning to the heart and reduce arterial vascular resistance and systolic pressure. Exercise caution when treating patients with any of the following conditions: blood volume depletion, existing hypotension, cardiomyopathies, congestive heart failure, acute myocardial infarction, or poor cardiac function for other reasons. If patients with any of these conditions are treated with nitroglycerin ointment, 0.4%, monitor cardiovascular status and clinical condition. The adverse reactions of nitroglycerin ointment, 0.4% are likely to be more pronounced in the elderly. 5.2 Headache Nitroglycerin ointment, 0.4% produces dose-related headaches, which may be severe. Tolerance to headaches occurs.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The most common adverse reaction of nitroglycerin ointment, 0.4% applied to the anal canal is headache. Headache may be recurrent following each dose. Headaches are typically of short duration and can be treated with an analgesic, e.g. acetaminophen, and are reversible upon discontinuation of treatment. In Study REC-C-001, a double-blind, placebo-controlled trial in patients with a painful chronic anal fissure, the most frequent (≥ 2%) adverse reactions reported were as follows (Table 1): Table 1: Incidence of Adverse Reactions (≥ 2%) in Study REC-C-001 Nitroglycerin Ointment N = 123 Placebo N = 124 System Organ Class Preferred term Patients n (%) Events n Patients n (%) Events n Nervous system disorders Headache 79 (64) 938 51 (41) 225 Dizziness 6 (5) 26 0 0 Most common adverse reactions are headache and dizziness. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact TruPharma LLC at 1-877-541-5504 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Hypotension Transient episodes of light-headedness, occasionally related to blood pressure changes, also may occur. Hypotension (including orthostatic hypotension) occurs infrequently, but in some patients may be severe enough to warrant discontinuation of therapy. Allergic Reactions Flushing, allergic reactions, and application site reactions (including drug rash and exfoliative dermatitis) have been reported rarely. Methemoglobinemia In rare cases, therapeutic doses of organic nitrates have caused methemoglobinemia (see 10 OVERDOSAGE ).
adverse reactions table
<table><caption>Table 1: Incidence of Adverse Reactions (≥ 2%) in Study REC-C-001</caption><col width="46.789%"/><col width="18.124%"/><col width="11.542%"/><col width="12.002%"/><col width="11.542%"/><tbody><tr><td styleCode="Botrule Lrule Rrule Toprule" valign="top"/><td colspan="2" align="center" styleCode="Botrule Rrule Toprule" valign="top"><content styleCode="bold">Nitroglycerin Ointment</content> <content styleCode="bold">N = 123</content></td><td colspan="2" align="center" styleCode="Botrule Rrule Toprule" valign="top"><content styleCode="bold">Placebo</content> <content styleCode="bold">N = 124</content></td></tr><tr><td styleCode="Botrule Lrule Rrule" valign="top"><content styleCode="bold">System Organ Class</content> Preferred term </td><td align="center" styleCode="Botrule Rrule" valign="top"><content styleCode="bold">Patients</content> <content styleCode="bold">n (%)</content></td><td align="center" styleCode="Botrule Rrule" valign="top"><content styleCode="bold">Events</content> <content styleCode="bold">n</content></td><td align="center" styleCode="Botrule Rrule" valign="top"><content styleCode="bold">Patients</content> <content styleCode="bold">n (%)</content></td><td align="center" styleCode="Botrule Rrule" valign="top"><content styleCode="bold">Events</content> <content styleCode="bold">n</content></td></tr><tr><td styleCode="Botrule Lrule Rrule" valign="top"><content styleCode="bold">Nervous system disorders</content></td><td colspan="4" align="center" styleCode="Botrule Rrule" valign="top"/></tr><tr><td styleCode="Botrule Lrule Rrule" valign="top"> Headache</td><td align="center" styleCode="Botrule Rrule" valign="top">79 (64)</td><td align="center" styleCode="Botrule Rrule" valign="top">938</td><td align="center" styleCode="Botrule Rrule" valign="top">51 (41)</td><td align="center" styleCode="Botrule Rrule" valign="top">225</td></tr><tr><td styleCode="Botrule Lrule Rrule" valign="top"> Dizziness</td><td align="center" styleCode="Botrule Rrule" valign="top">6 (5)</td><td align="center" styleCode="Botrule Rrule" valign="top">26</td><td align="center" styleCode="Botrule Rrule" valign="top">0</td><td align="center" styleCode="Botrule Rrule" valign="top">0</td></tr></tbody></table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.