NDC codes

FDA NDC Directory
Product NDC (as listed)72241-002Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72241-0002Add 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
72241-002-047224100020490 TABLET, COATED in 1 BOTTLE (72241-002-04)Marketed from Aug 19, 2021
72241-002-0572241000205100 TABLET, COATED in 1 BOTTLE (72241-002-05)Marketed from Aug 19, 2021

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)
Nateglinide
Generic name (nonproprietary)
nateglinide
Active ingredients
Nateglinide — 60 mg/1
Dosage form
Tablet, Coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206432
Marketing start
Listing expires
Other FDA classes
Potassium Channel Antagonists (Mechanism)
Identifiers
Product ID 72241-002_af81465b-5f49-4eeb-8122-ef7fe5d90ddcSPL ID af81465b-5f49-4eeb-8122-ef7fe5d90ddcSPL set ID af81465b-5f49-4eeb-8122-ef7fe5d90ddcRxCUI 311919, 314142UNII 41X3PWK4O2
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

N472241000204 followed by a unit qualifier and the quantity

Package 72241-0002-04. 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)

Nateglinide tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Limitations of Use : Nateglinide tablets should not be used in patients with type 1 diabetes mellitus or for the treatment of diabetic ketoacidosis. Nateglinide is a glinide indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( 1 ) Limitations of Use : Not for treating type 1 diabetes mellitus or diabetes ketoacidosis ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 206432

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

FDA NDC Directory listings under ANDA 206432
ProductStrengthForm · routeLabelerProduct NDC
NateglinideNateglinide 120 mg/1Tablet, CoatedOralModavar Pharmaceuticals LLC72241-003
NateglinideNateglinide 60 mg/1Tablet, CoatedOralCadila Pharmaceuticals Limited71209-030
NateglinideNateglinide 120 mg/1Tablet, CoatedOralCadila Pharmaceuticals Limited71209-031

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Nateglinide NDC 72241-002 | Med-Code