Drugplain

SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) 2.5 mg/mL

SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) · INJECTION, SOLUTION · HF Acquisition Co LLC, DBA HealthFirst

No Recall History
Plain English

SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) is a injection, solution containing sensorcaine(r) (bupivacaine hci and epinephrine) at 2.5 mg/mL, taken infiltration. Manufactured by HF Acquisition Co LLC, DBA HealthFirst.

Key Facts

Brand Name
SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE)
Generic Name
SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE)
NDC Code (Product)
51662-1397
Manufacturer
HF Acquisition Co LLC, DBA HealthFirst
Strength
2.5 mg/mL
Dosage Form
INJECTION, SOLUTION
Route
INFILTRATION, PERINEURAL
Marketing Status
Application #
ANDA070967
Marketing Start
10/08/2019

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS & USAGE Sensorcaine (bupivacaine HCl) is indicated for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Only the 0.25% and 0.5% concentrations are indicated for obstetrical anesthesia (see WARNINGS ). Experience with nonobstetrical surgical procedures in pregnant patients is not sufficient to recommend use of the 0.75% concentration of bupivacaine HCl in these patients. Sensorcaine is not recommended for intravenous regional anesthesia (Bier Block) (see WARNINGS ). The routes of administration and indicated Sensorcaine concentrations are: (See DOSAGE & ADMINISTRATION for additional information.) Standard textbooks should be consulted to determine the accepted procedures and techniques for the administration of Sensorcaine. INDICATIONS and USAGE

Dosage & Administration

DOSAGE & ADMINISTRATION The dose of any local anesthetic administered varies with the anesthetic procedure, the area to be anesthetized, the vascularity of the tissues, the number of neuronal segments to be blocked, the depth of anesthesia and degree of muscle relaxation required, the duration of anesthesia desired, individual tolerance, and the physical condition of the patient. The smallest dose and concentration required to produce the desired result should be administered. Dosages of Sensorcaine should be reduced for elderly and/or debilitated patients and patients with cardiac and/or liver disease. The rapid injection of a large volume of local anesthetic solution should be avoided and fractional (incremental) doses should be used when feasible. For specific techniques and procedures, refer to standard textbooks. There have been adverse event reports of chondrolysis in patients receiving intra-articular infusions of local anesthetics following arthroscopic and other surgical procedures. Sensorcaine is not approved for this use (see WARNINGS and DOSAGE & ADMINISTRATION ). In recommended doses, Sensorcaine (bupivacaine HCl) produces complete sensory block, but the effect on moto

Warnings

WARNINGS Methemoglobinemia: Cases of methemoglobinemia have been reported in association with local anesthetic use. Although all patients are at risk for methemoglobinemia, patients with glucose-6-phosphate dehydrogenase deficiency, congenital or idiopathic methemoglobinemia, cardiac or pulmonary compromise, infants under 6 months of age, and concurrent exposure to oxidizing agents or their metabolites are more susceptible to developing clinical manifestations of the condition. If local anesthetics must be used in these patients, close monitoring for symptoms and signs of methemoglobinemia is recommended. Signs of methemoglobinemia may occur immediately or may be delayed some hours after exposure, and are characterized by a cyanotic skin discoloration and/or abnormal coloration of the blood. Methemoglobin levels may continue to rise; therefore, immediate treatment is required to avert more serious central nervous system and cardiovascular adverse effects, including seizures, coma, arrhythmias, and death. Discontinue Sensorcaine and any other oxidizing agents. Depending on the severity of the signs and symptoms, patients may respond to supportive care, i.e., oxygen therapy, hydratio

Contraindications

CONTRAINDICATIONS Sensorcaine (bupivacaine HCl) is contraindicated in obstetrical paracervical block anesthesia. Its use in this technique has resulted in fetal bradycardia and death. Sensorcaine is contraindicated in patients with a known hypersensitivity to it or to any local anesthetic agent of the amide-type or to other components of bupivacaine solutions.

Adverse Reactions

ADVERSE REACTIONS Reactions to Sensorcaine (bupivacaine HCl) are characteristic of those associated with other amide- type local anesthetics. A major cause of adverse reactions to this group of drugs is excessive plasma levels, which may be due to overdosage, unintentional intravascular injection, or slow metabolic degradation. The most commonly encountered acute adverse experiences which demand immediate counter-measures are related to the central nervous system and the cardiovascular system. These adverse experiences are generally dose related and due to high plasma levels which may result from overdosage, rapid absorption from the injection site, diminished tolerance, or from unintentional intravascular injection of the local anesthetic solution. In addition to systemic dose-related toxicity, unintentional subarachnoid injection of drug during the intended performance of caudal or lumbar epidural block or nerve blocks near the vertebral column (especially in the head and neck region) may result in underventilation or apnea (“Total or High Spinal”). Also, hypotension due to loss of sympathetic tone and respiratory paralysis or underventilation due to cephalad extension of the mot

Frequently Asked Questions

What is SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) used for?

SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) contains SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE). It is a injection, solution taken infiltration. Consult your doctor for specific uses.

Is SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) a controlled substance?

SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) is not classified as a controlled substance by the DEA.

What is the generic name for SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE)?

The generic name for SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) is SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE). There are no other listed brand versions of SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE).

What is the NDC code for SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) 2.5 mg/mL?

The NDC (National Drug Code) for SENSORCAINE(R) (BUPIVACAINE HCI AND EPINEPHRINE) 2.5 mg/mL is 51662-1397, listed by HF Acquisition Co LLC, DBA HealthFirst.

Product NDC

51662-1397

Package NDC

51662-1397-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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