Cefzil

[Cefprozil]

Renal Impairment

Cefprozil may be administered to patients with impaired renal function. The following dosage schedule should be used.
Creatinine Clearance Dosage Dosing Interval (mL/ min) (mg)

30Ð 120 standard standard 0Ð 29* 0 50% of standard standard
* Cefprozil is in part removed by hemodialysis; therefore, cefprozil should be adminis-tered after the completion of hemodialysis.

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Hepatic Impairment

No dosage adjustment is necessary for patients with impaired hepatic function.

HOW SUPPLIED

CEFZIL ® (cefprozil) Tablets
Each light orange film-coated tablet, imprinted with "7720" on one side and "250" on the other, contains the equivalent of 250 mg anhydrous cefprozil.
Bottles of 100 Tablets NDC 0087-7720-60 Each white film-coated tablet, imprinted with "7721" on one side and "500" on the
other, contains the equivalent of 500 mg anhydrous cefprozil. Bottles of 50 Tablets
NDC 0087-7721-50 Bottles of 100 Tablets NDC 0087-7721-60

Store at controlled room temperature, 59° to 86° F (15° to 30° C).
CEFZIL ® (cefprozil) For Oral Suspension Each 5 mL of constituted suspension contains the equivalent of 125 mg anhydrous

cefprozil. 50 mL Bottle
NDC 0087-7718-40 75 mL Bottle NDC 0087-7718-62

100 mL Bottle NDC 0087-7718-64 Each 5 mL of constituted suspension contains the equivalent of 250 mg anhydrous cefprozil. 50 mL Bottle NDC 0087-7719-40 75 mL Bottle NDC 0087-7719-62

100 mL Bottle NDC 0087-7719-64 All powder formulations for oral suspension contain cefprozil in a bubble-gum flavored mixture.
Reconstitution Directions for Oral Suspension Prepare the suspension at the time of dispensing; for ease in preparation, add water in two portions and shake well after each aliquot.
Total Amount of Water Required for Reconstitution

After mixing, store in a refrigerator and discard unused portion after 14 days. Store at 59° to 77° F (15° to 25° C) prior to constitution.
U. S. Patent No. 4,520,022

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