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
- 37808-049_f0fcbeef-9c57-79cb-e053-2a95a90aa504
- Product NDC
- 37808-049
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Naproxen Sodium
- Labeler
- HEB
- Marketing category
- NDA
- Marketing start / end (source format)
- 20190101
- 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, PLASTIC in 1 CARTON (37808-049-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-049-15
- 1 BOTTLE, PLASTIC in 1 CARTON (37808-049-16) / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-049-16
- 1 BOTTLE, PLASTIC in 1 CARTON (37808-049-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-049-78
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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