United States · FDA National Drug Code directory

up and up naproxen sodium pm

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: 11673-687_6590fad1-9ef5-4613-9d82-dc958d53f0a5
Product NDC: 11673-687
Form: TABLET, FILM COATED
Composition / generic term: diphenhydramine hydrochloride, naproxen sodium
Labeler: Target Corporation
Marketing category: ANDA
Marketing start / end (source format): 20220125
Source listing expiry: 20261231

Source-listed ingredients

DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (11673-687-27) / 80 TABLET, FILM COATED in 1 BOTTLE · 11673-687-27

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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