United States · FDA National Drug Code directory
arthritis pain reliever
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
- 37808-087_a0bb2dd0-1a91-452e-83dd-61c717c39530
- Product NDC
- 37808-087
- Form
- GEL
- Composition / generic term
- diclofenac sodium
- Labeler
- H E B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200806
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 10 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (37808-087-01) / 100 g in 1 TUBE · 37808-087-01
- 1 TUBE in 1 CARTON (37808-087-02) / 50 g in 1 TUBE · 37808-087-02
- 1 TUBE in 1 CARTON (37808-087-03) / 150 g in 1 TUBE · 37808-087-03
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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