United States · FDA National Drug Code directory

Naproxen

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
76420-787_14060e9c-4605-5493-e063-6294a90ab6d3
Product NDC
76420-787
Form
TABLET
Composition / generic term
Naproxen
Labeler
Asclemed USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200301
Source listing expiry
20261231

Source-listed ingredients

  • NAPROXEN — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TABLET in 1 BOTTLE (76420-787-01) · 76420-787-01
  • 2 TABLET in 1 BOTTLE (76420-787-02) · 76420-787-02
  • 500 TABLET in 1 BOTTLE (76420-787-05) · 76420-787-05
  • 7 TABLET in 1 BOTTLE (76420-787-07) · 76420-787-07
  • 100 TABLET in 1 BOTTLE (76420-787-10) · 76420-787-10
  • 14 TABLET in 1 BOTTLE (76420-787-14) · 76420-787-14
  • 20 TABLET in 1 BOTTLE (76420-787-20) · 76420-787-20
  • 30 TABLET in 1 BOTTLE (76420-787-30) · 76420-787-30
  • 60 TABLET in 1 BOTTLE (76420-787-60) · 76420-787-60
  • 90 TABLET in 1 BOTTLE (76420-787-90) · 76420-787-90

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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