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labetalol hydrochloride tablet film coated

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.

cardinal health


3 years ago ROUND YELLOW 7 98 labetalol hydrochloride tablet film coated

ROUND YELLOW 7 98

HOW SUPPLIED

LABETALOL HYDROCHLORIDE Tablets, USP for oral administration are available as:

LABETALOL HYDROCHLORIDE Tablets USP, 100 mg are yellow colored, round, biconvex, film-coated tablets debossed with "7" and "98" on either side of score line on one side and plain on other side and are supplied as: Overbagged with 10 tablets per bag, NDC 55154-8192-0

LABETALOL HYDROCHLORIDE Tablets USP should be stored at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. FOR YOUR PROTECTION: Do not use if blister is torn or broken. To report SUSPECTED ADVERSE REACTIONS, contact Zydus Pharmaceuticals (USA) Inc. at 1-877-993-8779 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . This product's package insert may have been updated. For current package insert, call American Health Packaging at 1-800-707-4621. PACKAGING INFORMATION American Health Packaging unit dose blisters (see HOW SUPPLIED section) contain drug product from bluePoint Laboratories as follows: (100 mg / 100UD) NDC 60687-439-01 packaged from NDC 68001-381 (200 mg / 100UD) NDC 60687-450-01 packaged from NDC 68001-382 (300 mg / 100UD) NDC 60687-461-01 packaged from NDC 68001-383 Distributed by: American Health Packaging Columbus, OH 43217 Distributed By: Cardinal Health Dublin, OH 43017 L56924390224 8443901/0823


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