United States · FDA National Drug Code directory

Cefprozil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
57237-037_ccfc6236-d155-4a97-8cbf-a5d4592e677f
Product NDC
57237-037
Form
TABLET, FILM COATED
Composition / generic term
Cefprozil
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20070524
Source listing expiry
20261231

Source-listed ingredients

  • CEFPROZIL — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (57237-037-01) · 57237-037-01
  • 50 TABLET, FILM COATED in 1 BOTTLE (57237-037-50) · 57237-037-50

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Cefprozil — United States | Molindra Medicines