Benazepril hydrochloride 20 MG Hydrochlorothiazide 25 MG Oral Tablet

INDICATIONS AND USAGE Benazepril hydrochloride and hydrochlorothiazide tablets are indicated for the treatment of hypertension. This fixed combination drug is not indicated for the initial therapy of hypertension (see DOSAGE AND ADMINISTRATION ).

Eon Labs, Inc.

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

4 years ago

OVAL RED E277

HOW SUPPLIED

BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE Tablets, USP for oral administration, are available as 5 mg/6.25 mg white to off-white, oblong, film-coated tablets, debossed " E 124" on one side and scored on the other side and supplied as: NDC 0185-0236-01 bottles of 100 10 mg/12.5 mg pink, oblong, film-coated tablets, debossed " E 204" on one side and scored on the other side and supplied as: NDC 0185-0325-01 bottles of 100 20 mg/12.5 mg Lavender, oblong, film-coated tablets, debossed " E 211" on one side and scored on the other side and supplied as: NDC 0185-0211-01 bottles of 100 20 mg/25 mg maroon, oblong, film-coated tablets, debossed " E 277" on one side and scored on the other side and supplied as: NDC 0185-0277-01 bottles of 100 Each strength is supplied in bottles that contain a desiccant. Dispense in a tight, light-resistant container as defined in the USP with a child-resistant closure, as required. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from light and moisture. Keep tightly closed. KEEP OUT OF THE REACH OF CHILDREN. Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ 08540 Rev. July 2022 46309876

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benazepril 20 mg hydrochlorothiazide 12.5 mg

Eon Labs, Inc.

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