Over-the-counter drug · UNAPPROVED DRUG OTHER
Maximum Strength Urinary Pain Relief (Phenazopyridine hydrochloride) NDC 80513-517
Phenazopyridine hydrochloride 99.5 mg/1 · Tablet · Oral · Advanced Rx LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 80513-517-72 | 8051305177280513051772 | 72 TABLET in 1 BOTTLE (80513-517-72)Marketed from May 1, 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)
- Maximum Strength Urinary Pain Relief
- Generic name (nonproprietary)
- phenazopyridine hydrochloride
- Active ingredients
- Phenazopyridine hydrochloride — 99.5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Advanced Rx LLCNDC labeler code 80513
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 80513-517_1b87f423-20e1-743e-e063-6294a90aaa03SPL ID 1b87f423-20e1-743e-e063-6294a90aaa03SPL set ID a10464cf-36b2-460f-b31c-2e0edee3e4cfRxCUI 1094147UNII 0EWG668W17UPC 0380513001047
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
N480513051772followed by a unit qualifier and the quantityPackage 80513-0517-72. 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 Relief from urinary pain, burning, urgency and frequency associated with urinary tract infections.
Excerpt only. Read the full label for complete information.
About NDC 80513-517
- What is NDC 80513-517?
- 80513-517 is the product NDC for Maximum Strength Urinary Pain Relief, Phenazopyridine hydrochloride 99.5 mg/1 tablet, listed with the FDA by Advanced Rx LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Maximum Strength Urinary Pain Relief (Phenazopyridine Hydrochloride).
- What is the active ingredient?
- Phenazopyridine hydrochloride.
- Who is the labeler?
- Advanced Rx LLC, NDC labeler code 80513. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Maximum Strength Urinary Pain Relief?
- 2 other product NDCs are listed under this name. See all 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.
Related NDCs: other Maximum Strength Urinary Pain Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Maximum Strength Urinary Pain Reliefphenazopyridine hydrochloride | Phenazopyridine hydrochloride 99.5 mg/1 | TabletOral | TARGET CORPORATION | 11673-270 | 11673-0270-24 |
| Maximum Strength Urinary Pain Reliefphenazopyridine hydrochloride | Phenazopyridine hydrochloride 99.5 mg/1 | TabletOral | KROGER COMPANY | 30142-756 | 30142-0756-24 |