NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2321Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2321Add 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
71335-2321-171335232101713352321019 TABLET in 1 BOTTLE (71335-2321-1)Marketed from Jan 4, 2024
71335-2321-2713352321027133523210220 TABLET in 1 BOTTLE (71335-2321-2)Marketed from Jan 4, 2024
71335-2321-3713352321037133523210330 TABLET in 1 BOTTLE (71335-2321-3)Marketed from Jan 4, 2024
71335-2321-4713352321047133523210410 TABLET in 1 BOTTLE (71335-2321-4)Marketed from Jan 4, 2024
71335-2321-5713352321057133523210515 TABLET in 1 BOTTLE (71335-2321-5)Marketed from Jan 4, 2024
71335-2321-671335232106713352321066 TABLET in 1 BOTTLE (71335-2321-6)Marketed from Jan 4, 2024
71335-2321-7713352321077133523210790 TABLET in 1 BOTTLE (71335-2321-7)Marketed from Jan 4, 2024
71335-2321-8713352321087133523210812 TABLET in 1 BOTTLE (71335-2321-8)Marketed from Jan 4, 2024
71335-2321-9713352321097133523210918 TABLET in 1 BOTTLE (71335-2321-9)Marketed from Jan 4, 2024

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 hydrochloride
Active ingredients
Phenazopyridine hydrochloride — 200 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 71335-2321_55b0c95f-c150-418a-83a9-1708a517d1f5SPL ID 55b0c95f-c150-418a-83a9-1708a517d1f5SPL set ID 24786685-978b-4485-995a-2964802bc262RxCUI 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

N471335232101 followed by a unit qualifier and the quantity

Package 71335-2321-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Phenazopyridine Hydrochloride is indicated for the symptomatic relief of pain, burning, urgency frequency, and other discomforts arising from irritation of the mucosa of the lower urinary tract caused by infection, trauma, surgery, endoscopic procedures, or the passage of sounds or catheters. The use of Phenazopyridine Hydrochloride for relief of symptoms should not delay definitive diagnosis and treatment of causative conditions. The drug should be used for symptomatic relief of pain and not as a substitute for specific surgery or antimicrobial therapy. Phenazopyridine Hydrochloride is compatible with antimicrobial therapy and can help relieve pain and discomfort durin…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2321

What is NDC 71335-2321?
71335-2321 is the product NDC for Phenazopyridine Hydrochloride, Phenazopyridine hydrochloride 200 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phenazopyridine Hydrochloride.
What is the active ingredient?
Phenazopyridine hydrochloride.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phenazopyridine Hydrochloride?
48 other product NDCs are listed under this name. See all Phenazopyridine Hydrochloride 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 Phenazopyridine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 100 mg/1TabletOralGenus Lifesciences Inc.64950-55064950-0550-01
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 200 mg/1TabletOralGenus Lifesciences Inc.64950-55164950-0551-01
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 99.5 mg/1TabletOralGPT Pharmaceuticals Private Limited50696-00350696-0003-01
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 200 mg/1TabletOralPreferred Pharmaceuticals Inc68788-869568788-8695-0168788-8695-0268788-8695-05+1 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-866868788-8668-0168788-8668-0268788-8668-05+1 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 100 mg/1TabletOralREMEDYREPACK INC.70518-398670518-3986-0070518-3986-0170518-3986-02+2 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 200 mg/1TabletOralREMEDYREPACK INC.70518-397570518-3975-0070518-3975-0270518-3975-03+2 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 100 mg/1TabletOralProficient Rx LP82804-04782804-0047-0682804-0047-1082804-0047-12+6 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 100 mg/1TabletOralBryant Ranch Prepack71335-232371335-2323-0171335-2323-0271335-2323-03+6 more
Phenazopyridine HydrochloridePhenazopyridine hydrochloride 200 mg/1TabletOralProficient Rx LP82804-12582804-0125-0682804-0125-0982804-0125-10+1 more

All 49 Phenazopyridine Hydrochloride NDCs

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