Labetalol hydrochloride 100 MG Oral Tablet
INDICATIONS AND USAGE Labetalol hydrochloride tablets, USP are indicated in the management of hypertension. Labetalol hydrochloride tablets, USP may be used alone or in combination with other antihypertensive agents, especially thiazide and loop diuretics.
method pharmaceuticals, llc
ROUND BROWN I 126
I 126 ROUND BROWN
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HOW SUPPLIED
LABETALOL HYDROCHLORIDE Tablets, USP, for oral administration, are available as 100 mg round, beige film-coated tablets, plain on one side, scored and debossed with “I/126” on the other side: NDC 58657-602-01 bottles of 100 NDC 58657-602-50 bottles of 500 NDC 58657-602-10 bottles of 1000 200 mg round, white film-coated tablets, plain on one side, scored and debossed with “I/127” on the other side: NDC 58657-603-01 bottles of 100 NDC 58657-603-50 bottles of 500 NDC 58657-603-10 bottles of 1000 300 mg round, blue film-coated tablets, plain on one side, and debossed with “I/130” on the other side: NDC 58657-604-01 bottles of 100 NDC 58657-604-50 bottles of 500 NDC 58657-604-10 bottles of 1000
LABETALOL HYDROCHLORIDE Tablets, USP should be stored at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP with a child-resistant closure as required. To report SUSPECTED ADVERSE REACTI ONS, contact 1-844-466-6469 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . Distributed by: Method Pharmaceuticals, LLC Fort Worth, TX 76118 Rev. 11/2019
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