NDC codes

FDA NDC Directory
Product NDC (as listed)11673-028Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11673-0028Add 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
11673-028-10116730028101 TUBE in 1 CARTON (11673-028-10) / 100 g in 1 TUBEMarketed from Sep 1, 2026
11673-028-15116730028151 TUBE in 1 CARTON (11673-028-15) / 150 g in 1 TUBEMarketed from Sep 1, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 10 mg/g
Dosage form
Gel
Route
Topical
Labeler
Target CorporationNDC labeler code 11673
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204306
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 11673-028_44f66b1f-6634-4fe1-a988-5cbe70fe3b91SPL ID 44f66b1f-6634-4fe1-a988-5cbe70fe3b91

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

N411673002810 followed by a unit qualifier and the quantity

Package 11673-0028-10. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 11673-028

What is NDC 11673-028?
11673-028 is the product NDC for Diclofenac Sodium, Diclofenac sodium 10 mg/g gel, listed with the FDA by Target Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diclofenac Sodium.
What is the active ingredient?
Diclofenac sodium.
Who is the labeler?
Target Corporation, NDC labeler code 11673. 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 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
Diclofenac SodiumDiclofenac sodium 75 mg/1Tablet, Delayed releaseOralUmedica Laboratories USA Inc.60290-08460290-0084-0160290-0084-0260290-0084-03+1 more

All 240 Diclofenac Sodium NDCs

Other NDCs under ANDA 204306

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

FDA NDC Directory listings under ANDA 204306
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4335
Amazon Basic Care Arthritis Paindiclofenac sodiumDiclofenac sodium 10 mg/gGelTopicalAmazon.com Services LLC72288-624
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalINNOVUS PHARMACEUTICALS, INC.57483-185
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurobindo Pharma Limited84386-120
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalRedpharm Drug67296-2155
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalHarris Teeter72036-014
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurohealth LLC58602-604
Diclofenac Sodium—KitAurohealth LLC58602-606
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurohealth LLC58602-609
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalSportpharm LLC85766-137
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalKROGER COMPANY30142-277
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalGERI-CARE PHARMACEUTICAL CORP57896-147
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4135

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