Phenylephrine 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
- Phenylephrine Hydrochloride
- Generic name
- PHENYLEPHRINE HYDROCHLORIDE
- Manufacturer
- Fresenius Kabi USA, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b54a0c59-e5e4-4fd7-ba91-c991ce87b148
- SPL ID
- b54a0c59-e5e4-4fd7-ba91-c991ce87b148
- Version
- 1
- Effective date
- 2025-07-04
- 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 06:27:31
| Harmonized routes |
|---|
| 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 | 210665 | derived:openfda.application_number |
| application number | ANDA210665 | openfda.application_number | |
| brand name | Phenylephrine Hydrochloride | openfda.brand_name | |
| generic name | PHENYLEPHRINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Fresenius Kabi USA, LLC | openfda.manufacturer_name | |
| ndc | package | 65219-388-00 | openfda.package_ndc |
| ndc | package | 65219-388-01 | openfda.package_ndc |
| ndc | product | 65219-388 | openfda.product_ndc |
| ndc11 | package | 65219038800 | derived:openfda.package_ndc |
| ndc11 | package | 65219038801 | derived:openfda.package_ndc |
| rxcui | 1666372 | openfda.rxcui | |
| spl id | b54a0c59-e5e4-4fd7-ba91-c991ce87b148 | id | |
| spl set id | b54a0c59-e5e4-4fd7-ba91-c991ce87b148 | set_id | |
| unii | 04JA59TNSJ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS • Severe bradycardia and decreased cardiac output : ( 5.2 ) • Extravasation : during intravenous administration may cause necrosis or sloughing of tissue ( 5.4 ) • Concomitant use with oxytocic drugs : pressor effect of sympathomimetic pressor amines is potentiated ( 5.5 ) 5.1 Exacerbation of Angina, Heart Failure, or Pulmonary Arterial Hypertension Because of its pressor effects, phenylephrine hydrochloride can precipitate angina in patients with severe arteriosclerosis or history of angina, exacerbate underlying heart failure, and increase pulmonary arterial pressure. 5.2 Bradycardia Phenylephrine Hydrochloride Injection 10 mg/mL can cause severe bradycardia and decreased cardiac output. 5.3 Risk in Patients with Autonomic Dysfunction The pressor response to adrenergic drugs, including phenylephrine, can be increased in patients with autonomic dysfunction, as may occur with spinal cord injuries. 5.4 Skin and Subcutaneous Necrosis Extravasation of phenylephrine can cause necrosis or sloughing of tissue. 5.5 Pressor Effect with Concomitant Oxytocic Drugs Oxytocic drugs potentiate the pressor effect of sympathomimetic pressor amines including Phenylephrine Hydrochloride Injection 10 mg/mL [see Drug Interactions ( 7.1 )] , with the potential for hemorrhagic stroke. 5.7 Peripheral and Visceral Ischemia Phenylephrine Hydrochloride Injection 10 mg/mL can cause excessive peripheral and visceral vasoconstriction and ischemia to vital organs, particularly in patients with extensive peripheral vascular disease. 5.8 Renal Toxicity Phenylephrine Hydrochloride Injection 10 mg/mL can increase the need for renal replacement therapy in patients with septic shock. Monitor renal function.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS The following adverse reactions associated with the use of phenylephrine hydrochloride were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency reliably or to establish a causal relationship to drug exposure. Cardiac disorders : Bradycardia, AV block, ventricular extrasystoles, myocardial ischemia Gastrointestinal disorders : Nausea, vomiting General disorders and administrative site conditions : Chest pain, extravasation Immune system disorders : Sulfite sensitivity Nervous system disorders : Headache, nervousness, paresthesia, tremor Psychiatric disorders : Excitability Respiratory : Pulmonary edema, rales Skin and subcutaneous tissue disorders : Diaphoresis, pallor, piloerection, skin blanching, skin necrosis with extravasation Vascular disorders : Hypertensive crisis Most common adverse reactions: nausea and vomiting, headache, nervousness ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 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.