24 HR desvenlafaxine succinate 25 MG Extended Release Oral Tablet

1 INDICATIONS AND USAGE Desvenlafaxine extended-release tablets are indicated for the treatment of adults with major depressive disorder (MDD) [see Clinical Studies ( 14 )] . Desvenlafaxine extended-release tablets are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of adults with major depressive disorder (MDD) ( 1 ).

actavis pharma, inc.

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

4 years ago

SQUARE PINK A112

16 HOW SUPPLIED/STORAGE AND HANDLING

DESVENLAFAXINE extended-release tablets are available as follows: 25 mg, light pink, square, pyramid tablets imprinted with “A112” in black ink on one side NDC 0591-4060-30, bottle of 30 tablets in unit-of-use package 50 mg, light pink, square, pyramid tablets imprinted with “WPI” and “3659” in black ink on one side NDC 0591-3659-30, bottle of 30 tablets in unit-of-use package 100 mg, reddish-orange, square, pyramid tablets imprinted with “WPI” and “3660” in black ink on one side NDC 0591-3660-30, bottle of 30 tablets in unit-of-use package Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Each tablet contains 38 mg, 76 mg or 152 mg of

DESVENLAFAXINE succinate equivalent to 25 mg, 50 mg or 100 mg of

DESVENLAFAXINE, respectively.

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24 HR desvenlafaxine succinate 25 MG Extended Release Oral Tablet

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

SQUARE PINK A112

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