opana er oxymorphone hydrochloride 10 mg tablet film coated extended release
INDICATIONS AND USAGE OPANA ER is indicated for the relief of moderate to severe pain in patients requiring continuous, around-the-clock opioid treatment for an extended period of time. OPANA ER is not intended for use as a prn analgesic. OPANA ER is not indicated for pain in the immediate post-operative period (12-24 hours following surgery) for patients not previously taking opioids because of the risk of oversedation and respiratory depression requiring reversal with opioid antagonists. OPANA ER is not indicated for pain in the post-operative period if the pain is mild or not expected to persist for an extended period of time.
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OCTAGON ORANGE E674 10
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HOW SUPPLIED OPANA ER tablets are supplied as follows: 5 mg pink, octagon shape, film coated, convex tablets with “E907” over “5” in black print on one side and plain on the other. Bottles of 100 with child-resistant closure NDC 63481-907-70 Unit-Dose package of 100 tablets (5 blister cards of 20 tablets, not child-resistant, for hospital use only) NDC 63481-907-75 10 mg Light orange, octagon shape, film coated, convex tablets with “E674” over “10” in black print on one side and plain on the other. Bottles of 100 with child-resistant closure NDC 63481-674-70 Unit-Dose package of 100 tablets (5 blister cards of 20 tablets, not child-resistant, for hospital use only) NDC 63481-674-75 20 mg Light green, octagon shape, film coated, convex tablets with “E617” over “20” in black print on one side and plain on the other. Bottles of 100 with child-resistant closure NDC 63481-617-70 Unit-Dose package of 100 tablets (5 blister cards of 20 tablets, not child-resistant, for hospital use only) NDC 63481-617-75 40 mg yellow, octagon shape, film coated, convex tablets with “E693” over “40” in black print on one side and plain on the other. Bottles of 100 with child-resistant closure NDC 63481-693-70 Unit-Dose package of 100 tablets (5 blister cards of 20 tablets, not child-resistant, for hospital use only) NDC 63481-693-75 Rx Only CAUTION DEA Order Form Required.
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