What is NDC 72090-072?

72090-072 is the product NDC for Gencare-Urinary Pain Relief Maximum Strength, Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gencare-Urinary Pain Relief Maximum Strength (Phenazopyridine hydrochloride).

Pioneer Life Sciences, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gencare-Urinary Pain Relief Maximum Strength?

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.

NDC 72090-072

NDC codes

FDA NDC Directory

Product NDC (as listed)72090-072Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72090-0072Add 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
72090-072-01	7209000720172090007201	3 BLISTER PACK in 1 CARTON (72090-072-01) / 24 TABLET in 1 BLISTER PACKMarketed from Jul 21, 2026

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): Gencare-Urinary Pain Relief Maximum Strength
Generic name (nonproprietary): phenazopyridine hydrochloride
Active ingredients: Phenazopyridine hydrochloride — 99.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Pioneer Life Sciences, LLCNDC labeler code 72090
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jul 21, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 72090-072_2b8a7cdc-5f20-4628-acdd-17d0b58cbac7SPL ID 2b8a7cdc-5f20-4628-acdd-17d0b58cbac7SPL set ID 6bbf15b4-2954-40ff-8460-1ef0ed890654RxCUI 1094147UNII 0EWG668W17UPC 0372090001909

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

N472090007201 followed by a unit qualifier and the quantity

Package 72090-0072-01. 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 Aug 3, 2026.

Indications (excerpt from the label)

Use Relief from urinary pain, burning, urgency and frequency associated with urinary tract infections.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72090-072

What is NDC 72090-072?: 72090-072 is the product NDC for Gencare-Urinary Pain Relief Maximum Strength, Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gencare-Urinary Pain Relief Maximum Strength (Phenazopyridine hydrochloride).
What is the active ingredient?: Phenazopyridine hydrochloride.
Who is the labeler?: Pioneer Life Sciences, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gencare-Urinary Pain Relief Maximum Strength?: 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.

Gencare-Urinary Pain Relief Maximum Strength (Phenazopyridine hydrochloride) NDC 72090-072