United States · FDA National Drug Code directory

RELAFEN DS

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
15370-170_48aa3640-1dd2-4693-9b0d-a99595b97a0e
Product NDC
15370-170
Form
TABLET
Composition / generic term
NABUMETONE
Labeler
Carwin Pharmaceutical Associates, LLC
Marketing category
ANDA
Marketing start / end (source format)
20190920
Source listing expiry
20261231

Source-listed ingredients

  • NABUMETONE — 1000 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (15370-170-10) · 15370-170-10
  • 30 TABLET in 1 BOTTLE, PLASTIC (15370-170-30) · 15370-170-30
  • 60 TABLET in 1 BOTTLE, PLASTIC (15370-170-60) · 15370-170-60
  • 1 BLISTER PACK in 1 CARTON (15370-170-99) / 2 TABLET in 1 BLISTER PACK · 15370-170-99

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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