HYDRALAZINE HYDROCHLORIDE
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
- HYDRALAZINE HYDROCHLORIDE
- Generic name
- HYDRALAZINE HYDROCHLORIDE
- Manufacturer
- Meitheal Pharmaceuticals Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f3c806a4-b971-421c-bcb9-9979c6d7aaec
- SPL ID
- 2926d221-0ca5-4379-ac53-773051ec5c79
- Version
- 4
- Effective date
- 2026-02-27
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:14
| Harmonized routes |
|---|
| INTRAMUSCULAR, INTRAVENOUS |
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 | 217501 | derived:openfda.application_number |
| application number | ANDA217501 | openfda.application_number | |
| brand name | HYDRALAZINE HYDROCHLORIDE | openfda.brand_name | |
| generic name | HYDRALAZINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Meitheal Pharmaceuticals Inc. | openfda.manufacturer_name | |
| ndc | package | 71288-205-02 | openfda.package_ndc |
| ndc | package | 71288-205-01 | openfda.package_ndc |
| ndc | product | 71288-205 | openfda.product_ndc |
| ndc11 | package | 71288020502 | derived:openfda.package_ndc |
| ndc11 | package | 71288020501 | derived:openfda.package_ndc |
| rxcui | 966571 | openfda.rxcui | |
| spl id | 2926d221-0ca5-4379-ac53-773051ec5c79 | id | |
| spl set id | f3c806a4-b971-421c-bcb9-9979c6d7aaec | set_id | |
| unii | FD171B778Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS In a few patients hydralazine may produce a clinical picture simulating systemic lupus erythematosus including glomerulonephritis. In such patients hydralazine should be discontinued unless the benefit-to-risk determination requires continued antihypertensive therapy with this drug. Symptoms and signs usually regress when the drug is discontinued but residua have been detected many years later. Long-term treatment with steroids may be necessary (see PRECAUTIONS, Laboratory Tests ).
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Adverse reactions with hydralazine hydrochloride are usually reversible when dosage is reduced. However, in some cases it may be necessary to discontinue the drug. The following adverse reactions have been observed, but there has not been enough systematic collection of data to support an estimate of their frequency. Common: Headache, anorexia, nausea, vomiting, diarrhea, palpitations, tachycardia, angina pectoris. Less Frequent: Digestive : constipation, paralytic ileus. Cardiovascular : hypotension, paradoxical pressor response, edema. Respiratory : dyspnea Neurologic : peripheral neuritis, evidenced by paresthesia, numbness, and tingling; dizziness; tremors; muscle cramps; psychotic reactions characterized by depression, disorientation, or anxiety. Genitourinary : difficulty in urination. Hematologic : blood dyscrasias, consisting of reduction in hemoglobin and red cell count, leukopenia, agranulocytosis, purpura; lymphadenopathy; splenomegaly. Hypersensitive Reactions : rash, urticaria, pruritus, fever, chills, arthralgia, eosinophilia, and, rarely, hepatitis. Other : nasal congestion, flushing, lacrimation, conjunctivitis. To report SUSPECTED ADVERSE REACTIONS, contact Meitheal Pharmaceuticals Inc. at 1-844-824-8426 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . OVERDOSAGE Acute Toxicity: No deaths due to acute poisoning have been reported. Highest known dose survived: adults, 10 g orally. Oral LD 50 in rats: 173 and 187 mg/kg. Signs and Symptoms Signs and symptoms of overdosage include hypotension, tachycardia, headache, and generalized skin flushing. Complications can include myocardial ischemia and subsequent myocardial infarction, cardiac arrhythmia, and profound shock. Treatment There is no specific antidote. Support of the cardiovascular system is of primary importance. Shock should be treated with plasma expanders. If possible, vasopressors should not be given, but if a vasopressor is required, care should be taken not to precipitate or aggravate cardiac arrhythmia. Tachycardia responds to beta blockers. Digitalization may be necessary, and renal function should be monitored and supported as required. No experience has been reported with extracorporeal or peritoneal dialysis.
adverse reactions table
<table width="100%" styleCode="Noautorules"><caption/><tbody><tr><td><content styleCode="bold">Common:</content></td><td>Headache, anorexia, nausea, vomiting, diarrhea, palpitations, tachycardia, angina pectoris.</td></tr><tr><td valign="top"><content styleCode="bold">Less Frequent:</content></td><td><content styleCode="italics">Digestive</content>: constipation, paralytic ileus. <content styleCode="italics">Cardiovascular</content><content styleCode="italics">:</content> hypotension, paradoxical pressor response, edema. <content styleCode="italics">Respiratory</content>: dyspnea <content styleCode="italics">Neurologic</content>: peripheral neuritis, evidenced by paresthesia, numbness, and tingling; dizziness; tremors; muscle cramps; psychotic reactions characterized by depression, disorientation, or anxiety. <content styleCode="italics">Genitourinary</content>: difficulty in urination. <content styleCode="italics">Hematologic</content><content styleCode="italics">:</content> blood dyscrasias, consisting of reduction in hemoglobin and red cell count, leukopenia, agranulocytosis, purpura; lymphadenopathy; splenomegaly. <content styleCode="italics">Hypersensitive Reactions</content><content styleCode="italics">:</content> rash, urticaria, pruritus, fever, chills, arthralgia, eosinophilia, and, rarely, hepatitis. <content styleCode="italics">Other</content><content styleCode="italics">:</content> nasal congestion, flushing, lacrimation, conjunctivitis.</td></tr></tbody></table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.