NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2386Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2386Add 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
72162-2386-172162238601100 TABLET in 1 CONTAINER (72162-2386-1)Marketed from Aug 15, 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)
Probenecid
Generic name (nonproprietary)
probenecid
Active ingredients
Probenecid — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217020
Marketing start
Listing expires
Identifiers
Product ID 72162-2386_c2638148-9137-410b-b35b-671a77b52412SPL ID c2638148-9137-410b-b35b-671a77b52412SPL set ID a4f4b3e1-44a9-4b3a-9f7f-f9749ed451caRxCUI 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

N472162238601 followed by a unit qualifier and the quantity

Package 72162-2386-01. 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

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