United States · FDA National Drug Code directory
Diclofenac Potassium
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
- 67877-772_2b2c8805-3cf1-48f8-9612-8a72a30a7f20
- Product NDC
- 67877-772
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Diclofenac Potassium
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221024
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC POTASSIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 PACKET in 1 CARTON (67877-772-58) / 1 POWDER, FOR SOLUTION in 1 PACKET (67877-772-49) · 67877-772-58
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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