loperamide hydrochloride capsule

INDICATIONS AND USAGE Loperamide hydrochloride is indicated for the control and symptomatic relief of acute nonspecific diarrhea in patients 2 years of age and older and of chronic diarrhea in adults associated with inflammatory bowel disease. Loperamide hydrochloride capsules are also indicated for reducing the volume of discharge from ileostomies.

Teva Pharmaceuticals USA, Inc.

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] adverse drug reaction` `[3] nausea` `[4] fatigue` `[5] off label use` `[6] diarrhoea` `[7] headache` `[8] toxicity to various agents` `[9] completed suicide` `[10] dyspnoea`

4 years ago

CAPSULE BROWN TEVA 0311

HOW SUPPLIED

LOPERAMIDE HYDROCHLORIDE capsules USP, 2 mg are available as: A light brown opaque body and dark brown opaque capsule, imprinted "TEVA" on the cap and "0311" on the body and packaged in bottles of 100 (NDC 0093-0311-01) and 500 (NDC 0093-0311-05). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a well-closed container, as defined in the USP, with a child-resistant closure (as required). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. Manufactured In Czech Republic By: Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic Manufactured For: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454 Rev. Q 11/2016

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loperamide hydrochloride capsule

teva pharmaceuticals usa, inc.

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loperamide hydrochloride capsule

FDA Reported Adverse Reactions [1] drug ineffective [2] adverse drug reaction [3] nausea [4] fatigue [5] off label use [6] diarrhoea [7] headache [8] toxicity to various agents [9] completed suicide [10] dyspnoea

CAPSULE BROWN TEVA 0311

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loperamide hydrochloride capsule

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] adverse drug reaction` `[3] nausea` `[4] fatigue` `[5] off label use` `[6] diarrhoea` `[7] headache` `[8] toxicity to various agents` `[9] completed suicide` `[10] dyspnoea`