NDC codes

FDA NDC Directory
Product NDC (as listed)68788-4335Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-4335Add 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
68788-4335-1687884335011 TUBE in 1 CARTON (68788-4335-1) / 100 g in 1 TUBEMarketed from Jul 2, 2026

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 — 10 mg/g
Dosage form
Gel
Route
Topical
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 68788-4335_09643e65-f301-4891-96f4-d78bf3621e23SPL ID 09643e65-f301-4891-96f4-d78bf3621e23SPL set ID 09643e65-f301-4891-96f4-d78bf3621e23RxCUI 855633UNII 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

N468788433501 followed by a unit qualifier and the quantity

Package 68788-4335-01. 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 .

Indications (excerpt from the label)

Uses • for the temporary relief of arthritis pain ONLY in the following areas: o hand, wrist, elbow (upper body areas) o foot, ankle, knee (lower body areas) • this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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
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/gGelTopicalHarris Teeter72036-014
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurobindo Pharma Limited84386-120
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/gGelTopicalKROGER COMPANY30142-277
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalRedpharm Drug67296-2155
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalSportpharm LLC85766-137
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalGERI-CARE PHARMACEUTICAL CORP57896-147
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4135

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