NDC codes

FDA NDC Directory
Product NDC (as listed)85509-1911Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85509-1911Add 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
85509-1911-1855091911011 BOTTLE in 1 CARTON (85509-1911-1) / 150 mL in 1 BOTTLEMarketed from Oct 23, 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
Active ingredients
Diclofenac sodium — 16.05 mg/mL
Dosage form
Solution
Route
Topical
Labeler
PHOENIX RX LLCNDC labeler code 85509
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206116
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 85509-1911_41daa6f6-41c5-b81e-e063-6394a90a7516SPL ID 41daa6f6-41c5-b81e-e063-6394a90a7516SPL set ID 41dab520-5651-a4c5-e063-6394a90a2962RxCUI 857700UNII 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

N485509191101 followed by a unit qualifier and the quantity

Package 85509-1911-01. 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 signs and symptoms of osteoarthritis of the knee(s). Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug indicated for the treatment of signs and symptoms 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)

About NDC 85509-1911

What is NDC 85509-1911?
85509-1911 is the product NDC for Diclofenac Sodium (diclofenac), Diclofenac sodium 16.05 mg/mL solution, listed with the FDA by PHOENIX RX LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diclofenac Sodium (Diclofenac).
What is the active ingredient?
Diclofenac sodium.
Who is the labeler?
PHOENIX RX LLC, NDC labeler code 85509. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diclofenac Sodium?
239 other product NDCs are listed under this name. See all Diclofenac Sodium NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Diclofenac Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diclofenac Sodiumdiclofenac sodium topical gel, 1%Diclofenac sodium 10 mg/gGelTopicalIPG Pharmaceuticals, inc.71085-08471085-0084-03
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalTarget Corporation11673-02811673-0028-1011673-0028-15
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralNorthwind Health Company, LLC82868-11482868-0114-30
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-413568788-4135-01
Diclofenac SodiumDiclofenac sodium 100 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited84386-10384386-0103-01
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralREMEDYREPACK INC.70518-469470518-4694-00
Diclofenac sodiumDiclofenac sodium 30 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-411868788-4118-01
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-433568788-4335-01
Diclofenac SodiumDiclofenac sodium 25 mg/1Tablet, Delayed releaseOralUmedica Laboratories USA Inc.60290-08260290-0082-01
Diclofenac SodiumDiclofenac sodium 50 mg/1Tablet, Delayed releaseOralUmedica Laboratories USA Inc.60290-08360290-0083-0160290-0083-0260290-0083-03+1 more

All 240 Diclofenac Sodium NDCs

Other NDCs under ANDA 206116

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

FDA NDC Directory listings under ANDA 206116
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalProficient Rx LP71205-811
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-0237
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalDIRECT RX72189-075
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalAsclemed USA, Inc.76420-012
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalA-S Medication Solutions50090-3316
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalPreferred Pharmaceuticals Inc.68788-7270
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalAdvanced Rx of Tennessee, LLC80425-0368
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalDirect_Rx72189-527
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalAmneal Pharmaceuticals LLC65162-911
Diclofenac SodiumDiclofenac sodium 16.05 mg/mLSolutionTopicalSOLA Pharmaceuticals, LLC70512-810
Diclofenac SodiumdiclofenacDiclofenac sodium 16.05 mg/mLSolutionTopicalBryant Ranch Prepack72162-2031

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