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minoxidil 2.5 MG Oral Tablet

INDICATIONS AND USAGE Because of the potential for serious adverse effects, minoxidil tablets are indicated only in the treatment of hypertension that is symptomatic or associated with target organ damage and is not manageable with maximum therapeutic doses of a diuretic plus two other antihypertensive drugs. At the present time use in milder degrees of hypertension is not recommended because the benefit-risk relationship in such patients has not been defined. Minoxidil reduced supine diastolic blood pressure by 20 mm Hg or to 90 mm Hg or less in approximately 75% of patients, most of who had hypertension that could not be controlled by other drugs.

Actavis Pharma, Inc.

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

4 weeks ago ROUND WHITE DAN 5642 2 5 minoxidil 2.5 MG Oral Tablet

ROUND WHITE DAN 5642 2 5

4 weeks ago ROUND WHITE DAN 5642 2 5 minoxidil 2.5 MG Oral Tablet

DAN 5642 2 5 ROUND WHITE

HOW SUPPLIED

MINOXIDIL Tablets, USP 2.5 mg are 9/32 ", scored, round, white tablets imprinted “ DAN 5642 ” and “ 2.5 ” supplied in bottles of 100 NDC 0591-5642-01 and 500 NDC 0591-5642-05.

MINOXIDIL Tablets, USP 10 mg are 9/32 ", scored, round, white tablets imprinted “ DAN 5643 ” and “ 10 ” supplied in bottles of 100 NDC 0591-5643-01 and 500 NDC 0591-5643-05. Dispense in a tight container with child-resistant closure. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Dispense with Patient Package Insert available at: www.tevausa.com/PatientPI Manufactured In India By: Watson Pharma Private Limited Verna, Salcette Goa 403 722, India Manufactured For: Teva Pharmaceuticals Parsippany, NJ 07054 Rev. B 2/2024


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