NDC codes

FDA NDC Directory
Product NDC (as listed)72036-014Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72036-0014Add 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
72036-014-1072036001410720360014101 TUBE in 1 CARTON (72036-014-10) / 100 g in 1 TUBEMarketed from Aug 26, 2024
72036-014-5072036001450720360014501 TUBE in 1 CARTON (72036-014-50) / 50 g in 1 TUBEMarketed from Aug 26, 2024

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
Harris TeeterNDC labeler code 72036
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 72036-014_cd769edb-b4e5-4f62-9e0e-91c6b6718bf2SPL ID cd769edb-b4e5-4f62-9e0e-91c6b6718bf2SPL set ID 17ed520d-bfbe-4a33-e063-6394a90aa0f6RxCUI 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

N472036001410 followed by a unit qualifier and the quantity

Package 72036-0014-10. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses for the temporary relief of arthritis pain ONLY in the following areas: hand, wrist, elbow (upper body areas) 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)

About NDC 72036-014

What is NDC 72036-014?
72036-014 is the product NDC for Diclofenac Sodium, Diclofenac sodium 10 mg/g gel, listed with the FDA by Harris Teeter. 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?
Harris Teeter, NDC labeler code 72036. 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?
241 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 242 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
Amazon Basic Care Arthritis Paindiclofenac sodiumDiclofenac sodium 10 mg/gGelTopicalAmazon.com Services LLC72288-624
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalTarget Corporation11673-028
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalKROGER COMPANY30142-277
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalINNOVUS PHARMACEUTICALS, INC.57483-185
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalGERI-CARE PHARMACEUTICAL CORP57896-147
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/gGelTopicalRedpharm Drug67296-2155
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4135
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalPreferred Pharmaceuticals Inc.68788-4335
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalAurobindo Pharma Limited84386-120
Diclofenac SodiumDiclofenac sodium 10 mg/gGelTopicalSportpharm LLC85766-137

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