NDC codes

FDA NDC Directory
Product NDC (as listed)68788-7778Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-7778Add 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
68788-7778-368788777803687887778031 BLISTER PACK in 1 CARTON (68788-7778-3) / 12 TABLET in 1 BLISTER PACKMarketed from Jun 4, 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

Generic name (nonproprietary)
phenazopyridine hydrochloride
Active ingredients
Phenazopyridine hydrochloride — 99.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 68788-7778_0fa8638c-e3e0-4bbf-9101-842e5d8736d6SPL ID 0fa8638c-e3e0-4bbf-9101-842e5d8736d6SPL set ID 0fa8638c-e3e0-4bbf-9101-842e5d8736d6RxCUI 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

N468788777803 followed by a unit qualifier and the quantity

Package 68788-7778-03. 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 .

Indications (excerpt from the label)

Use 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 68788-7778

What is NDC 68788-7778?
68788-7778 is the product NDC for Preferred Maximum Strength Urinary Pain Relief, Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Preferred Maximum Strength Urinary Pain Relief (Phenazopyridine hydrochloride).
What is the active ingredient?
Phenazopyridine hydrochloride.
Who is the labeler?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Preferred Maximum Strength Urinary Pain Relief?
1 other product NDC are listed under this name. See all Preferred Maximum Strength Urinary Pain Relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Preferred Maximum Strength Urinary Pain Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Preferred Maximum Strength Urinary Pain Reliefphenazopyridine hydrochloridePhenazopyridine hydrochloride 99.5 mg/1TabletOralReese Pharmaceutical Co10956-21010956-0210-1210956-0210-24

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