United States · FDA National Drug Code directory

AnaDent

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
27854-170_44b15331-802d-46a2-9e1b-1f03708ec70d
Product NDC
27854-170
Form
TABLET, FILM COATED
Composition / generic term
Naproxen Sodium
Labeler
Belmora LLC
Marketing category
ANDA
Marketing start / end (source format)
20170123
Source listing expiry
20271231

Source-listed ingredients

  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 27854-170-01

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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