What is NDC 73436-2441?

73436-2441 is the product NDC for Uti Pain Relief (phenazopyridine hydrochloride), Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Cadence Health. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Uti Pain Relief (Phenazopyridine Hydrochloride).

Cadence Health, NDC labeler code 73436. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Uti Pain Relief?

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.

Uti Pain Relief NDC 73436-2441 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73436-2441Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73436-2441Add 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
73436-2441-2	7343624410273436244102	1 BLISTER PACK in 1 CARTON (73436-2441-2) / 12 TABLET in 1 BLISTER PACKMarketed from Apr 15, 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): Uti Pain Relief
Generic name (nonproprietary): phenazopyridine hydrochloride
Active ingredients: Phenazopyridine hydrochloride — 99.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cadence HealthNDC labeler code 73436
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 6, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 73436-2441_4ece86b2-06de-2cd8-e063-6294a90a5a7cSPL ID 4ece86b2-06de-2cd8-e063-6294a90a5a7cSPL set ID 7fa8e314-025c-46c2-b97a-91c4f385e565RxCUI 1094147UNII 0EWG668W17

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

NDC on a medical claim

N473436244102 followed by a unit qualifier and the quantity

Package 73436-2441-02. 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 Apr 6, 2026.

Indications (excerpt from the label)

Uses Fast relief from urinary pain, burning, urgency and frequency associated with urinary tract infections. Treatment should not exceed 2 days; see Directions

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73436-2441

What is NDC 73436-2441?: 73436-2441 is the product NDC for Uti Pain Relief (phenazopyridine hydrochloride), Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Cadence Health. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Uti Pain Relief (Phenazopyridine Hydrochloride).
What is the active ingredient?: Phenazopyridine hydrochloride.
Who is the labeler?: Cadence Health, NDC labeler code 73436. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Uti Pain Relief?: 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.

Uti Pain Relief (Phenazopyridine hydrochloride) NDC 73436-2441