What is NDC 72189-541?

72189-541 is the product NDC for Trubrexa Patch ER, Capsaicin .00025 g/g; Lidocaine .0475 g/g patch, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Trubrexa Patch ER?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Trubrexa Patch ER NDC 72189-541 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-541Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0541Add 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
72189-541-11	72189054111	2.7 g in 1 PATCH (72189-541-11)Marketed from Mar 11, 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): Trubrexa Patch ER
Generic name (nonproprietary): trubrexa patch er
Active ingredients: Capsaicin — .00025 g/gLidocaine — .0475 g/g
Dosage form: Patch
Route: Transdermal
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Mar 11, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 72189-541_1367f190-670b-d2de-e063-6394a90abb13SPL ID 1367f190-670b-d2de-e063-6394a90abb13SPL set ID 1367f190-670a-d2de-e063-6394a90abb13RxCUI 2667457UNII S07O44R1ZM, 98PI200987
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

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. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472189054111 followed by a unit qualifier and the quantity

Package 72189-0541-11. 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 Mar 11, 2024.

Indications (excerpt from the label)

Trubrexa TM Transdermal Patch is indicated in adults over the age of 12 years old for the treatment of acute and chronic pain in muscles and joints associated with muscle soreness, strains, sprains, arthritis, simple backache, muscle stiffness, and more.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-541

What is NDC 72189-541?: 72189-541 is the product NDC for Trubrexa Patch ER, Capsaicin .00025 g/g; Lidocaine .0475 g/g patch, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Trubrexa Patch ER.
What is the active ingredient?: Capsaicin, Lidocaine.
Who is the labeler?: Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trubrexa Patch ER?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.