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
50844-604_89d3ed35-e75c-41d8-aa99-57cc1fd866d2
Product NDC
50844-604
Form
TABLET, FILM COATED
Composition / generic term
Naproxen Sodium
Labeler
L.N.K. International, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170201
Source listing expiry
20271231

Source-listed ingredients

  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06) · 50844-604-06
  • 4 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACK · 50844-604-09
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-14) · 50844-604-14
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-604-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-604-15
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-16) · 50844-604-16
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-604-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-604-19
  • 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-56) · 50844-604-56
  • 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-98) · 50844-604-98
  • 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-99) · 50844-604-99

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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