What is NDC 16571-831?

16571-831 is the product NDC for Probenecid, Probenecid 500 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Rising Pharma Holdings, Inc., NDC labeler code 16571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Probenecid?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Probenecid NDC 16571-831 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)16571-831Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16571-0831Add 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
16571-831-01	16571083101	100 TABLET in 1 CONTAINER (16571-831-01)Marketed from Nov 20, 2023
16571-831-10	16571083110	1000 TABLET in 1 CONTAINER (16571-831-10)Marketed from Nov 20, 2023

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): Probenecid
Generic name (nonproprietary): probenecid
Active ingredients: Probenecid — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Rising Pharma Holdings, Inc.NDC labeler code 16571
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217020
Marketing start: Nov 20, 2023
Listing expires: Dec 31, 2027
Identifiers: Product ID 16571-831_5b9e2e37-77b7-464f-9bc8-ff678643d773SPL ID 5b9e2e37-77b7-464f-9bc8-ff678643d773SPL set ID f2375d90-4132-4fb6-aee7-c4f9d11e98d5RxCUI 198152UNII PO572Z7917

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

N416571083101 followed by a unit qualifier and the quantity

Package 16571-0831-01. 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 Jan 28, 2026.

Indications (excerpt from the label)

INDICATIONS & USAGE Probenecid tablets are indicated for the treatment of the hyperuricemia associated with gout and gouty arthritis. As an adjuvant to therapy with penicillin or with ampicillin, methicillin, oxacillin, cloxacillin, or nafcillin, for elevation and prolongation of plasma levels by whatever route the antibiotic is given.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16571-831

What is NDC 16571-831?: 16571-831 is the product NDC for Probenecid, Probenecid 500 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Probenecid.
What is the active ingredient?: Probenecid.
Who is the labeler?: Rising Pharma Holdings, Inc., NDC labeler code 16571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Probenecid?: 6 other product NDCs are listed under this name. See all Probenecid 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 Probenecid NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Probenecid	Probenecid 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-4649	70518-4649-00
Probenecid	Probenecid 500 mg/1	TabletOral	Bryant Ranch Prepack	72162-2386	72162-2386-01
Probenecid	Probenecid 500 mg/1	Tablet, Film coatedOral	Actavis Pharma, Inc.	0591-5347	00591-5347-0100591-5347-10
Probenecid	Probenecid 500 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1367	00527-1367-0100527-1367-10
Probenecid	Probenecid 500 mg/1	Tablet, Film coatedOral	Marlex Pharmaceuticals Inc	10135-541	10135-0541-0110135-0541-10
Probenecid	Probenecid 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2237	72162-2237-01

Other NDCs under ANDA 217020

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 217020
Product	Strength	Form · route	Labeler	Product NDC
Probenecid	Probenecid 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-4649
Probenecid	Probenecid 500 mg/1	TabletOral	Bryant Ranch Prepack	72162-2386