What is NDC 37012-098?

37012-098 is the product NDC for Skopko Urinary Pain Relief (phenazopyridine hydrochloride), Phenazopyridine hydrochloride 95 mg/1 tablet, listed with the FDA by Skopko. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Skopko Urinary Pain Relief (Phenazopyridine hydrochloride).

Skopko, NDC labeler code 37012. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Skopko Urinary 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.

Skopko Urinary Pain Relief NDC 37012-098

NDC codes

FDA NDC Directory

Product NDC (as listed)37012-098Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37012-0098Add 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
37012-098-01	3701200980137012009801	1 CELLO PACK in 1 CARTON (37012-098-01) / 32 TABLET in 1 CELLO PACK (37012-098-50)Marketed from Jul 1, 2013
37012-098-30	3701200983037012009830	30 TABLET in 1 CELLO PACK (37012-098-30)Marketed from Jul 1, 2013

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): Skopko Urinary Pain Relief
Generic name (nonproprietary): phenazopyridine hydrochloride
Active ingredients: Phenazopyridine hydrochloride — 95 mg/1
Dosage form: Tablet
Route: Oral
Labeler: SkopkoNDC labeler code 37012
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jul 1, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 37012-098_0e0edb43-c2af-45ef-9bb0-264a65367ed6SPL ID 0e0edb43-c2af-45ef-9bb0-264a65367ed6SPL set ID dc614b08-461c-4e29-8e5a-eccfdd680cefRxCUI 1094126UNII 0EWG668W17UPC 0400081004506

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

N437012009801 followed by a unit qualifier and the quantity

Package 37012-0098-01. 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 Dec 18, 2024.

Indications (excerpt from the label)

Uses fast 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 37012-098

What is NDC 37012-098?: 37012-098 is the product NDC for Skopko Urinary Pain Relief (phenazopyridine hydrochloride), Phenazopyridine hydrochloride 95 mg/1 tablet, listed with the FDA by Skopko. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Skopko Urinary Pain Relief (Phenazopyridine hydrochloride).
What is the active ingredient?: Phenazopyridine hydrochloride.
Who is the labeler?: Skopko, NDC labeler code 37012. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Skopko Urinary 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.

Skopko Urinary Pain Relief (Phenazopyridine hydrochloride) NDC 37012-098