3 Background Drug Information Drug: OxyContin (oxycodone hydrochloride (HCl) extended-release) Original FDA Approval Date: Decem
Class 4 Medicines Defect Information: OxyContin 20 mg prolonged release tablets Drug alert number: Date issued: OxyContin 20 mg prolonged release tablets (PL
Approval Date: . Indications: For the management of moderate to severe pain OxyContin (Oxycodone Hydrochloride Controlled-Release) Tablets
Generic OxyContin Availability. Last updated on . OxyContin is a brand name of oxycodone, approved by the FDA in the following formulation(s): OXYCONTIN (oxycodone hydrochloride - tablet, extended release;oral) Manufacturer: PURDUE PHARMA LP Approval date: Ap
Cosmetic Act (FDCA), for OXYCONTIN (oxycodone hydrochloride) extended-release tablets. date(s). We request that the labeling approved
Up to Date. This article was reviewed by a medical professional to OxyContin is a controlled-release formulation of oxycodone, meaning it works
Generic OxyContin Availability. Last updated on . OxyContin is a brand name of oxycodone, approved by the FDA in the following formulation(s): OXYCONTIN (oxycodone hydrochloride - tablet, extended release;oral) Manufacturer: PURDUE PHARMA LP Approval date: Ap
Generic OxyContin Availability. Last updated on . OxyContin is a brand name of oxycodone, approved by the FDA in the following formulation(s): OXYCONTIN (oxycodone hydrochloride - tablet, extended release;oral) Manufacturer: PURDUE PHARMA LP Approval date: Ap
Generic OxyContin Availability. Last updated on . OxyContin is a brand name of oxycodone, approved by the FDA in the following formulation(s): OXYCONTIN (oxycodone hydrochloride - tablet, extended release;oral) Manufacturer: PURDUE PHARMA LP Approval date: Ap
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