Diclofenac Sodium NDC 72603-207

NDC codes

FDA NDC Directory

Product NDC (as listed)72603-207Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72603-0207Add 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 NDC	11-digit (billing)	Package	Copy
72603-207-01	72603020701	1 BOTTLE in 1 CARTON (72603-207-01) / 112 g in 1 BOTTLEMarketed from Jun 1, 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 — 20 mg/g
Dosage form: Solution
Route: Topical
Labeler: NorthStar Rx LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213040
Marketing start: Jun 1, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers: Product ID 72603-207_e3058adb-1a77-4e85-bcc2-78fa045bde77SPL ID e3058adb-1a77-4e85-bcc2-78fa045bde77SPL set ID fd467c1a-6463-4d92-9960-3e308c733edbRxCUI 1487074UNII QTG126297QUPC 0372603207019
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N472603020701 followed by a unit qualifier and the quantity

Package 72603-0207-01. 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 Jan 10, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

1. INDICATIONS AND USAGE 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 213040

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

FDA NDC Directory listings under ANDA 213040
Product	Strength	Form · route	Labeler	Product NDC
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	A-S Medication Solutions	50090-7632
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	Proficient Rx LP	82804-160
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	Preferred Pharmaceuticals Inc.	68788-8541
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	Aurolife Pharma LLC	13107-269
Diclofenac Sodium Topical Solution	Diclofenac sodium 20 mg/g	SolutionTopical	Direct_Rx	72189-546
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	Asclemed USA, Inc	76420-861
Diclofenac Sodium	Diclofenac sodium 20 mg/g	SolutionTopical	Proficient Rx LP	82804-074