NDC codes

FDA NDC Directory
Product NDC (as listed)72189-546Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0546Add 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
72189-546-0472189054604112 g in 1 BOTTLE (72189-546-04)Marketed from Apr 10, 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 Topical Solution
Generic name (nonproprietary)
diclofenac sodium topical solution
Active ingredients
Diclofenac sodium — 20 mg/g
Dosage form
Solution
Route
Topical
Labeler
Direct_Rx
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213040
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Prostaglandin Production (Physiologic effect)
Identifiers
Product ID 72189-546_15c2cd6d-b7c3-d927-e063-6394a90aa63eSPL ID 15c2cd6d-b7c3-d927-e063-6394a90aa63eSPL set ID 15c2cd6d-b7c2-d927-e063-6394a90aa63eRxCUI 1487074UNII 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

N472189054604 followed by a unit qualifier and the quantity

Package 72189-0546-04. 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 the pain of osteoarthritis of the knee(s).

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
ProductStrengthForm · routeLabelerProduct NDC
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalNorthStar Rx LLC72603-207
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalA-S Medication Solutions50090-7632
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalProficient Rx LP82804-160
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalPreferred Pharmaceuticals Inc.68788-8541
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalAurolife Pharma LLC13107-269
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalAsclemed USA, Inc76420-861
Diclofenac SodiumDiclofenac sodium 20 mg/gSolutionTopicalProficient Rx LP82804-074

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