buprenorphine 8.64 mg

1 INDICATIONS AND USAGE Buprenorphine sublingual tablet is indicated for the treatment of opioid dependence and is preferred for induction. Buprenorphine sublingual tablet should be used as part of a complete treatment plan to include counseling and psychosocial support. Buprenorphine sublingual tablet, contains buprenorphine, a partial opioid agonist, and is indicated for the treatment of opioid dependence and is preferred for induction. (1) Buprenorphine sublingual tablet should be used as part of a complete treatment plan that includes counseling and psychosocial support. (1)

sun pharmaceutical industries, inc.

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] pain` `[3] fatigue` `[4] off label use` `[5] nausea` `[6] headache` `[7] dyspnoea` `[8] rash` `[9] arthralgia` `[10] diarrhoea`

3 years ago

ROUND WHITE 460

3 years ago

460 ROUND WHITE

16 HOW SUPPLIED / STORAGE AND HANDLING

BUPRENORPHINE sublingual tablets containing 2 mg

BUPRENORPHINE (as the free base, equivalent to 2.16 mg

BUPRENORPHINE hydrochloride USP) are uncoated, round, biconvex, white to off-white, sublingual tablets, debossed with ‘459’ on one side and plain on other side and are supplied as: Bottles of 30 with child-resistant cap……………..NDC 62756-459-83 Unit-Dose blister pack of 30 (3×10) tablets ……..... NDC 62756-459-64

BUPRENORPHINE sublingual tablets containing 8 mg

BUPRENORPHINE (as the free base, equivalent to 8.64 mg

BUPRENORPHINE hydrochloride USP) are uncoated, round, biconvex, white to off-white, sublingual tablets, debossed with ‘460’ on one side and plain on other side and are supplied as: Bottles of 30 with child-resistant cap……………..NDC 62756-460-83 Unit-Dose blister pack of 30 (3×10) tablets ……..... NDC 62756-460-64 Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° and 30°C (59° and 86°F) [see USP Controlled Room Temperature]. Protect from light. Store

BUPRENORPHINE sublingual tablets securely and dispose of properly [see Patient Counseling Information (17)] .

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