labetalol hydrochloride 200 mg

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.

innogenix, inc.

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

2 years ago

ROUND WHITE I 127

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 and supplied as: NDC 71247-126-01 bottles of 100 NDC 71247-126-05 bottles of 500 200 mg : round, white, film-coated tablets, plain on one side, scored and debossed with “I/127” on the other side and supplied as: NDC 71247-127-01 bottles of 100 NDC 71247-127-05 bottles of 500 300 mg : round, blue, film-coated tablets, plain on one side and debossed with “I/130” on the other side and supplied as: NDC 71247-130-01 bottles of 100 NDC 71247-130-05 bottles of 500

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 REACTIONS, contact Innogenix, LLC. at 1-844-466-6469 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Distributed by: Innogenix, LLC. Amityville, NY 11701 Rev. 09/2020

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labetalol hydrochloride 200 mg

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

ROUND WHITE I 127

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