Phenylephrine Hydrochloride PHENYLEPHRINE HYDROCHLORIDE FRESENIUS KABI USA, LLC FDA Approved Phenylephrine Hydrochloride Injection contain active pharmaceutical ingredient phenylephrine in the form of hydrochloride salt. Phenylephrine is a synthetic sympathomimetic agent in sterile form for parenteral injection. Chemically, phenylephrine hydrochloride is (-)- m -Hydroxy-α-[(methylamino)methyl]benzyl alcohol hydrochloride and has the following structural formula: Phenylephrine hydrochloride is very soluble in water, freely soluble in ethanol, and insoluble in chloroform and ethyl ether. Phenylephrine hydrochloride is sensitive to light. Phenylephrine Hydrochloride Injection, USP is a clear, colorless, aqueous solution that is essentially free of visible foreign matter. It MUST BE DILUTED before administration as bolus intravenous infusion or continuous intravenous infusion. Each mL contains: Phenylephrine Hydrochloride 10 mg; Sodium Chloride 3.5 mg; Sodium Citrate Dihydrate 4 mg; and Citric Acid 1 mg in water for injection. The pH may be adjusted in the range of 3.5 to 5.5 with Sodium Hydroxide and/or Hydrochloric Acid, if necessary. Structural Formula
FunFoxMeds bottle
Route
INTRAVENOUS
Applications
ANDA210665

Drug Facts

Composition & Profile

Dosage Forms
Injection
Strengths
10 mg/ml 1 ml 01 unit
Quantities
1 ml
Treats Conditions
1 Indications And Usage Phenylephrine Hydrochloride Injection 10 Mg Ml Is Indicated For Increasing Blood Pressure In Adults With Clinically Important Hypotension Resulting Primarily From Vasodilation In The Settings Of Anesthesia And Septic Shock Phenylephrine Hydrochloride Injection 10 Mg Ml Is Alpha 1 Adrenergic Receptor Agonist Indicated For Increasing Blood Pressure In Adults With Clinically Important Hypotension Resulting Primarily From Vasodilation In The Settings Of Anesthesia And Septic Shock

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
04JA59TNSJ
Packaging

16 HOW SUPPLIED/STORAGE AND HANDLING Phenylephrine Hydrochloride Injection, USP, is supplied as follows: Product Code Unit of Sale Strength Each RF751101 NDC 65219-388-01 Unit of 25 10 mg per mL NDC 65219-388-00 1 mL Single Dose Vial This product is RFID enabled. 751101 NDC 63323-751-01 Unit of 25 10 mg per mL NDC 63323-751-00 1 mL Single Dose Vial Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. Keep covered in carton until time of use. For single use only. Discard unused portion.; PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label NDC 63323-751-00 751101 Phenylephrine Hydrochloride Injection, USP 10 mg per mL For Intravenous Use Dilute Before Use DISCARD UNUSED PORTION PROTECT FROM LIGHT 1 mL Single Dose Vial Rx only PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label; PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Tray Label NDC 63323-751-01 751101 Phenylephrine Hydrochloride Injection, USP 10 mg per mL For Intravenous Use Dilute Before Use DISCARD UNUSED PORTION Rx only 25 x 1 mL Single Dose Vials PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label

Package Descriptions
  • 16 HOW SUPPLIED/STORAGE AND HANDLING Phenylephrine Hydrochloride Injection, USP, is supplied as follows: Product Code Unit of Sale Strength Each RF751101 NDC 65219-388-01 Unit of 25 10 mg per mL NDC 65219-388-00 1 mL Single Dose Vial This product is RFID enabled. 751101 NDC 63323-751-01 Unit of 25 10 mg per mL NDC 63323-751-00 1 mL Single Dose Vial Store at 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. Keep covered in carton until time of use. For single use only. Discard unused portion.
  • PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label NDC 63323-751-00 751101 Phenylephrine Hydrochloride Injection, USP 10 mg per mL For Intravenous Use Dilute Before Use DISCARD UNUSED PORTION PROTECT FROM LIGHT 1 mL Single Dose Vial Rx only PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label
  • PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Tray Label NDC 63323-751-01 751101 Phenylephrine Hydrochloride Injection, USP 10 mg per mL For Intravenous Use Dilute Before Use DISCARD UNUSED PORTION Rx only 25 x 1 mL Single Dose Vials PACKAGE LABEL- PRINCIPAL DISPLAY – Phenylephrine 1 mL Vial Label

Overview

Phenylephrine Hydrochloride Injection contain active pharmaceutical ingredient phenylephrine in the form of hydrochloride salt. Phenylephrine is a synthetic sympathomimetic agent in sterile form for parenteral injection. Chemically, phenylephrine hydrochloride is (-)- m -Hydroxy-α-[(methylamino)methyl]benzyl alcohol hydrochloride and has the following structural formula: Phenylephrine hydrochloride is very soluble in water, freely soluble in ethanol, and insoluble in chloroform and ethyl ether. Phenylephrine hydrochloride is sensitive to light. Phenylephrine Hydrochloride Injection, USP is a clear, colorless, aqueous solution that is essentially free of visible foreign matter. It MUST BE DILUTED before administration as bolus intravenous infusion or continuous intravenous infusion. Each mL contains: Phenylephrine Hydrochloride 10 mg; Sodium Chloride 3.5 mg; Sodium Citrate Dihydrate 4 mg; and Citric Acid 1 mg in water for injection. The pH may be adjusted in the range of 3.5 to 5.5 with Sodium Hydroxide and/or Hydrochloric Acid, if necessary. Structural Formula

Indications & Usage

Phenylephrine Hydrochloride Injection 10 mg/mL is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the settings of anesthesia and septic shock. Phenylephrine Hydrochloride Injection 10 mg/mL is alpha-1 adrenergic receptor agonist indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the settings of anesthesia and septic shock.

Dosage & Administration

• MUST BE DILUTED before administration. ( 2.1 ) Dosing for Perioperative Hypotension • Intravenous bolus administration: 50 mcg to 250 mcg ( 2.2 ) • Intravenous continuous infusion: 0.5 mcg/kg/minute to 1.4 mcg/kg/minute titrated to effect ( 2.2 ) Dosing for Patients with Vasodilatory Shock • Intravenous continuous infusion: 0.5 mcg/kg/minute to 6 mcg/kg/minute titrated to effect ( 2.2 ) 2.1 General Administration Instructions • Phenylephrine Hydrochloride Injection 10 mg/mL MUST BE DILUTED before administration as an intravenous bolus or for continuous intravenous infusion. The diluted solution should not be held for more than 4 hours at room temperature or for more than 24 hours under refrigerated conditions (2°C – 8°C). Parenteral drug products should be inspected for particulate matter and discoloration prior to administration. Discard any unused portion. During Phenylephrine Hydrochloride Injection 10 mg/mL administration: • Correct intravascular volume depletion. • Correct acidosis. Acidosis may reduce the effectiveness of phenylephrine. 2.2 Preparation of Phenylephrine Hydrochloride Injection Preparing a 100 mcg/mL Solution for Intravenous Bolus Administration For intravenous bolus administration, withdraw 10 mg (1 mL of a 10 mg/mL concentration) of Phenylephrine Hydrochloride Injection 10 mg/mL and dilute with 99 mL of 5% Dextrose Injection, USP or 0.9% Sodium Chloride Injection, USP. This will yield a final concentration of 100 mcg/mL. Withdraw an appropriate dose from the 100 mcg/mL solution prior to intravenous bolus administration. Preparing a 20 mcg/mL Solution for Continuous Intravenous Infusion For continuous intravenous infusion, withdraw 10 mg (1 mL of 10 mg/mL concentration) of phenylephrine hydrochloride injection 10 mg/mL and add to 500 mL of 5% Dextrose Injection, USP or 0.9% Sodium Chloride Injection, USP (providing a final concentration of 20 mcg/mL). Dosing for Perioperative Setting In adult patients undergoing surgical procedures with either neuraxial anesthesia or general anesthesia: • Phenylephrine Hydrochloride Injection 10 mg/mL (diluted to 20 mcg/mL): 0.5 mcg/kg/min to 1.4 mcg/kg/min by intravenous continuous infusion, titrated to blood pressure goal. Dosing for Septic or Other Vasodilatory Shock In adult patients with septic or other vasodilatory shock: • No bolus. • 0.5 mcg/kg/min to 6 mcg/kg/min by intravenous continuous infusion, titrated to blood pressure goal. Doses above 6 mcg/kg/min do not show significant incremental increase in blood pressure.

Warnings & 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.
Contraindications

The use of Phenylephrine Hydrochloride Injection 10 mg/mL is contraindicated in patients with: • Hypersensitivity to the product or any of its components • Hypersensitivity to the products or any of its components ( 4 )

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.

Drug Interactions

• Agonistic effects with monoamine oxidase inhibitors (MAOI), β-adrenergic blocking agents, α-2 adrenergic agonists, steroids, tricyclic antidepressants, norepinephrine transport inhibitors, ergot alkaloids, centrally-acting sympatholytic agents and atropine sulfate ( 7.1 ) • Antagonistic effects on and by α-adrenergic blocking agents ( 7.2 ) Agonists The pressor effect of phenylephrine hydrochloride is increased in patients receiving: • Monoamine oxidase inhibitors (MAOI), such as selegiline. • β-adrenergic blockers • α-2 adrenergic agonists, such as clonidine • Steroids • Tricyclic antidepressants • Norepinephrine transport inhibitors, such as atomoxetine • Ergot alkaloids, such as methylergonovine maleate • Centrally-acting sympatholytic agents, such as guanfacine or reserpine • Atropine sulfate 7.2 Antagonists α-adrenergic blocking agents, including phenothiazines (e.g., chlorpromazine) and amiodarone block phenylephrine and are in turn blocked by phenylephrine.


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