Prescription drug · UNAPPROVED DRUG OTHER
Phenazopyridine Hydrochloride (phenazopyridine) NDC 70518-3868
Phenazopyridine hydrochloride 200 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-3868-1 | 70518386801 | 21 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)Marketed from Sep 15, 2024 | |
| 70518-3868-3 | 70518386803 | 30 TABLET in 1 BLISTER PACK (70518-3868-3)Marketed from Mar 7, 2025 |
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)
- Phenazopyridine Hydrochloride
- Generic name (nonproprietary)
- phenazopyridine
- Active ingredients
- Phenazopyridine hydrochloride — 200 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 70518-3868_53e5fcb2-f144-3739-e063-6394a90a5da0SPL ID 53e5fcb2-f144-3739-e063-6394a90a5da0SPL set ID 82dc87bb-ba27-4b86-9bc9-18492975ac9fRxCUI 1094104UNII 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
N470518386801followed by a unit qualifier and the quantityPackage 70518-3868-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.