NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2598Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2598Add 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
71335-2598-17133525980130 TABLET in 1 BOTTLE (71335-2598-1)Marketed from Jun 5, 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)
Repaglinide
Generic name (nonproprietary)
repaglinide
Active ingredients
Repaglinide — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207209
Marketing start
Listing expires
Other FDA classes
Potassium Channel Antagonists (Mechanism)
Identifiers
Product ID 71335-2598_b117a9ea-a66f-4642-8f50-0f7d8bcae492SPL ID b117a9ea-a66f-4642-8f50-0f7d8bcae492SPL set ID d85abce4-16da-4231-b28a-6afca04ebf68RxCUI 200258UNII 668Z8C33LU
Pharmacologic class
Glinide

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

N471335259801 followed by a unit qualifier and the quantity

Package 71335-2598-01. 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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