buprenorphine and naloxone 2 mg

1 INDICATIONS AND USAGE Buprenorphine and naloxone sublingual tablets are indicated for the maintenance treatment of opioid dependence. Buprenorphine and naloxone sublingual tablets should be used as part of a complete treatment plan that includes counseling and psychosocial support. Buprenorphine and naloxone sublingual tablet contains buprenorphine, a partial opioid agonist, and naloxone, an opioid antagonist, and is indicated for the maintenance treatment of opioid dependence. ( 1 ) Buprenorphine and naloxone sublingual tablet should be used as part of a complete treatment plan that includes counseling and psychosocial support. ( 1 )

Lannett Company, Inc.

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] off label use` `[3] nausea` `[4] diarrhoea` `[5] fatigue` `[6] dyspnoea` `[7] product use in unapproved indication` `[8] pyrexia` `[9] pneumonia` `[10] headache`

8 months ago

HEXAGON PINK 2

8 months ago

2 HEXAGON PINK

16 HOW SUPPLIED/STORAGE AND HANDLING

BUPRENORPHINE AND NALOXONE sublingual tablets, USP are a hexagonal light pink tablet, debossed with a numeric imprint on one side identifying the strength, supplied in white HDPE bottles: NDC 62175-452-32 (buprenorphine 2 mg and naloxone 0.5 mg/sublingual tablet; content expressed in terms of free base) debossed with a 2 on one side - 30 tablets per bottle NDC 62175-458-32 (buprenorphine 8 mg and naloxone 2 mg/sublingual tablet; content expressed in terms of free base) debossed with an 8 on one side - 30 tablets per bottle Store at 25°C (77°F), excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature]. Store

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

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