NDC codes

FDA NDC Directory
Product NDC (as listed)85509-2406Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85509-2406Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
85509-2406-1855092406011 BOTTLE in 1 CARTON (85509-2406-1) / 112 g in 1 BOTTLEMarketed from Nov 14, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Diclofenac Sodium
Generic name (nonproprietary)
diclofenac sodium
Active ingredients
Diclofenac sodium — 20 mg/g
Dosage form
Solution
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207714
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 85509-2406_43926d0d-1675-d436-e063-6294a90a78baSPL ID 43926d0d-1675-d436-e063-6294a90a78baSPL set ID 4382cc15-8978-4f3b-e063-6394a90a9ecbRxCUI 1487074UNII QTG126297Q

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485509240601 followed by a unit qualifier and the quantity

Package 85509-2406-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Diclofenac sodium topical solution is indicated for the treatment of the pain of osteoarthritis of the knee(s). Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug indicated for the treatment of the pain of osteoarthritis of the knee(s). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207714

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 207714
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalApotex Corp.60505-0406
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalPreferred Pharmaceuticals Inc.68788-8838
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalPHOENIX RX LLC85509-1406
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalAdvanced Rx of Tennessee, LLC80425-0550

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