What is NDC 70518-4644?

70518-4644 is the product NDC for Probenecid and Colchicine, Probenecid 500 mg/1; Colchicine .5 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 and Colchicine?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Probenecid and Colchicine NDC 70518-4644

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4644Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4644Add 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
70518-4644-0	7051846440070518464400	50 POUCH in 1 BOX (70518-4644-0) / 1 TABLET in 1 POUCH (70518-4644-1)Marketed from Apr 28, 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

Brand name (proprietary): Probenecid and Colchicine
Generic name (nonproprietary): probenecid and colchicine
Active ingredients: Probenecid — 500 mg/1Colchicine — .5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217030
Marketing start: Apr 28, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Alkaloids (Chemical structure)
Identifiers: Product ID 70518-4644_5089d41d-851c-5a13-e063-6394a90a5e38SPL ID 5089d41d-851c-5a13-e063-6394a90a5e38SPL set ID 573e61e5-f5e1-4119-9d8e-d9a961a1baa9RxCUI 198153UNII PO572Z7917, SML2Y3J35T
Pharmacologic class: Alkaloid

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

N470518464400 followed by a unit qualifier and the quantity

Package 70518-4644-00. 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 Apr 28, 2026.

Indications (excerpt from the label)

INDICATIONS & USAGE For the treatment of chronic gouty arthritis when complicated by frequent, recurrent acute attacks of gout.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4644

What is NDC 70518-4644?: 70518-4644 is the product NDC for Probenecid and Colchicine, Probenecid 500 mg/1; Colchicine .5 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Probenecid and Colchicine.
What is the active ingredient?: Probenecid, Colchicine.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. 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 and Colchicine?: 2 other product NDCs are listed under this name. See all Probenecid and Colchicine 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 and Colchicine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Probenecid and Colchicine	Probenecid 500 mg/1; Colchicine .5 mg/1	TabletOral	Rising Pharma Holdings, Inc.	16571-832	16571-0832-01
Probenecid and Colchicine	Probenecid 500 mg/1; Colchicine .5 mg/1	TabletOral	Ingenus Pharmaceuticals, LLC	50742-263	50742-0263-01

Other NDCs under ANDA 217030

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

FDA NDC Directory listings under ANDA 217030
Product	Strength	Form · route	Labeler	Product NDC
Probenecid and Colchicine	Probenecid 500 mg/1; Colchicine .5 mg/1	TabletOral	Rising Pharma Holdings, Inc.	16571-832