OXYCODONE 30 MG HYDROCHLORIDE SUN

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OXYCODONE 30 MG HYDROCHLORIDE SUN

Oxycodone 30 mg Hydrochloride SUN, USP TABLETS ® tablets are an immediate-release oral formulation of oxycodone hydrochloride indicated forthe management of moderate to severe pain where the use of an opioid analgesic is appropriate.

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Buy Oxycodone 30 mg Hydrochloride SUN, USP Tablets Online.

Oxycodone 30 mg Hydrochloride SUN, ROXICODONE® (oxycodone hydrochloride tablets USP) is an opioid analgesic.

Each tablet for oral administration contains 5 mg, 15 mg or 30 mg of oxycodone hydrochloride USP.

Oxycodone hydrochloride is a white, odorless crystalline powder derived from the opium alkaloid, thebaine. Oxycodone hydrochloride dissolves in water(1 g in 6 to 7mL) and is considered slightly soluble in alcohol (octanol water partition coefcient is 0.7).

The 5 mg Roxicodone (oxycodone hydrochloride) tablet contains inactive ingredients:microcrystalline cellulose and stearic acid. The 15 and 30 mg tablets contain the following inactive ingredients: microcrystalline cellulose; sodium starch glycolate; corn starch; lactose; stearic acid; D&C Yellow No. 10 (15 mg tablet); and FD&C Blue No. 2 (15 mg and 30 mg tablets). The 5 mg, 15 mg and 30 mg tablets contain the equivalent of 4.6 mg, 13.5 mg and 27.0 mg,respectively, of oxycodone free base.

Buy Oxycodone 30 mg Hydrochloride SUN, USP Tablets Online

Oxycodone 30 mg Hydrochloride SUN, ROXICODONE® (oxycodone hydrochloride tablets USP) is an opioid analgesic.

Each tablet for oral administration contains 5 mg, 15 mg or 30 mg of oxycodone hydrochloride USP.

Oxycodone hydrochloride is a white, odorless crystalline powder derived from the opium alkaloid, thebaine. Oxycodone hydrochloride dissolves in water (1 g in 6 to 7 mL) and is considered slightly soluble in alcohol (octanol water partition coefficient is 0.7).

The 5 mg Roxicodone (oxycodone hydrochloride) tablet contains inactive ingredients: microcrystalline cellulose and stearic acid. The 15 and 30 mg tablets contain the following inactive ingredients: microcrystalline cellulose; sodium starch glycolate; corn starch; lactose; stearic acid; D&C Yellow No. 10 (15 mg tablet); and FD&C Blue No. 2 (15 mg and 30 mg tablets).

The 5 mg, 15 mg and 30 mg tablets contain the equivalent of 4.6 mg, 13.5 mg and 27.0 mg, respectively, of oxycodone free base.

INDICATIONS OXYCODONE 30 MG HYDROCHLORIDE SUN

ROXICODONE (oxycodone hydrochloride) ® tablets are an immediate-release oral formulation of oxycodone hydrochloride indicated for the management of moderate to severe pain where the use of an opioid analgesic is appropriate.

DOSAGE AND ADMINISTRATION

ROXICODONE (oxycodone hydrochloride) ® is intended forthe management of moderate to severe pain in patients who require treatment with an oral opioid analgesic. The dose should be individually adjusted according to severity of pain, patientresponse and patient size. If the pain increases in severity, if analgesia is not adequate, orif tolerance occurs, a gradual increase in dosage may be required. Patients who have not been receiving opioid analgesics should be started on ROXICODONE (oxycodone hydrochloride) ® in a dosing range of 5 to 15 mg every 4 to 6 hours as needed for pain. The dose should be titrated based upon the individual patient’s response to theirinitial dose of ROXICODONE (oxycodone hydrochloride) ®. Patients with chronic pain should have their dosage given on an aroundthe-clock basis to prevent the reoccurrence of pain ratherthan treating the pain afterit has occurred. This dose can then be adjusted to an acceptable level of analgesia taking into account side effects experienced by the patient.

 

PATIENTS CURRENTLY ON OPIOID THERAPY OXYCODONE 30 MG HYDROCHLORIDE SUN

If a patient has been receiving opioid-containing medications priorto taking ROXICODONE (oxycodone hydrochloride) ®, the potency of the prior opioid relative to oxycodone should be factored into the selection of the total daily dose (TDD) of oxycodone. In converting patients from other opioids to ROXICODONE (oxycodone hydrochloride) ® close observation and adjustment of dosage based upon the patient’s response to ROXICODONE oxycodone hydrochloride) ® is imperative. Administration of supplemental analgesia for breakthrough orincident pain and titration of the total daily
dose of ROXICODONE (oxycodone hydrochloride) ® may be necessary, especially in patients who have disease states that are changing rapidly.

MAINTENANCE OF THERAPY

Continual re-evaluation of the patientreceiving ROXICODONE (oxycodone hydrochloride) ® is important, with special attention to the maintenance of pain control and the relative incidence of side effects associated with therapy. If the level of pain increases, effort should be made to identify the ource of increased pain, while adjusting the dose as described above to decrease the level of pain. During chronic therapy, especially for non-cancer-related pain (or pain associated with otherterminal illnesses), the continued need forthe use of opioid analgesics should be re-assessed as appropriate.

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Tablets

100, 200, 300

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