United States · FDA National Drug Code directory
DICLOFENAC 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
- 57483-185_ad9d2c28-21bc-4f81-9c90-cce6a96d976a
- Product NDC
- 57483-185
- Form
- GEL
- Composition / generic term
- DICLOFENAC SODIUM
- Labeler
- INNOVUS PHARMACEUTICALS, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250325
- 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 (57483-185-11) / 150 g in 1 TUBE (57483-185-01) · 57483-185-11
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.
Browse United States records →