United States · FDA National Drug Code directory

Naproxen Sodium

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
21130-690_fe75f23c-9c5e-03a4-e053-6294a90a696d
Product NDC
21130-690
Form
TABLET
Composition / generic term
Naproxen Sodium
Labeler
BETTER LIVING BRANDS LLC.
Marketing category
ANDA
Marketing start / end (source format)
20230613
Source listing expiry
20261231

Source-listed ingredients

  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (21130-690-05) / 50 TABLET in 1 BOTTLE · 21130-690-05

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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