NDC codes

FDA NDC Directory
Product NDC (as listed)71610-949Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0949Add 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
71610-949-607161009496090 TABLET in 1 BOTTLE (71610-949-60)Marketed from Sep 17, 2025
71610-949-8071610094980180 TABLET in 1 BOTTLE (71610-949-80)Marketed from Sep 15, 2025

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)
Allopurinol
Generic name (nonproprietary)
allopurinol
Active ingredients
Allopurinol — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214443
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 71610-949_3f010fe3-b62e-40dd-e063-6294a90a2f7dSPL ID 3f010fe3-b62e-40dd-e063-6294a90a2f7dSPL set ID 3f0134bf-b62f-1077-e063-6394a90a60b0RxCUI 197319UNII 63CZ7GJN5I
Pharmacologic class
Xanthine Oxidase Inhibitor

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

N471610094960 followed by a unit qualifier and the quantity

Package 71610-0949-60. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 214443

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

FDA NDC Directory listings under ANDA 214443
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralHarman Finochem Limited82638-113
AllopurinolAllopurinol 100 mg/1TabletOralHarman Finochem Limited82638-112
AllopurinolAllopurinol 100 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-710
AllopurinolAllopurinol 100 mg/1TabletOralLeading Pharma, LLC69315-291
AllopurinolAllopurinol 300 mg/1TabletOralLeading Pharma, LLC69315-292
AllopurinolAllopurinol 200 mg/1TabletOralLeading Pharma, LLC69315-409
AllopurinolAllopurinol 300 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3672
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack71335-2542
AllopurinolAllopurinol 300 mg/1TabletOralCoupler LLC67046-1639
AllopurinolAllopurinol 300 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8713
AllopurinolAllopurinol 100 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3803
AllopurinolAllopurinol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8727

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