Cipro XR

[ciprofloxacin]

Impaired Hepatic Function:

No dosage adjustment is required with CIPRO XR in patients with stable chronic cirrhosis. The kinetics of ciprofloxacin in patients with acute hepatic insufficiency, however, have not been fully elucidated. (See CLINICAL PHARMACOLOGY, Special Populations.)

HOW SUPPLIED

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CIPRO XR is available as nearly white to slightly yellowish, film-coated, oblong-shaped tablets containing 500 mg or 1000 mg ciprofloxacin. The 500 mg tablet is coded with the word “BAYER” on one side and “C500 QD” on the reverse side. The 1000 mg tablet is coded with the word “BAYER” on one side and “C1000 QD” on the reverse side.

Strength NDC Code
Bottles of 30 500 mg 0026-8889-69
Bottles of 50 500 mg 0026-8889-50
Bottles of 100 500 mg 0026-8889-51

Bottles of 50 1000 mg 0026-8897-50
Bottles of 100
1000 mg 0026-8897-51
Unit Dose Pack of 30 1000 mg 0026-8897-69

Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature].

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