United States · FDA National Drug Code directory

Amoxicillin and Clavulanate Potassium

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
63187-032_83901ad8-02a3-41a4-8c1d-cda4378c3b15
Product NDC
63187-032
Form
TABLET, FILM COATED
Composition / generic term
Amoxicillin and Clavulanate Potassium
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20021031
Source listing expiry
20261231

Source-listed ingredients

  • AMOXICILLIN — 500 mg/1
  • CLAVULANATE POTASSIUM — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 TABLET, FILM COATED in 1 BOTTLE (63187-032-06) · 63187-032-06
  • 20 TABLET, FILM COATED in 1 BOTTLE (63187-032-20) · 63187-032-20
  • 21 TABLET, FILM COATED in 1 BOTTLE (63187-032-21) · 63187-032-21

Source and coverage

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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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