NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2416Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2416Add 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
71335-2416-171335241601100 TABLET in 1 BOTTLE (71335-2416-1)Marketed from Nov 12, 2024
71335-2416-27133524160230 TABLET in 1 BOTTLE (71335-2416-2)Marketed from Nov 12, 2024
71335-2416-37133524160360 TABLET in 1 BOTTLE (71335-2416-3)Marketed from Nov 12, 2024
71335-2416-471335241604120 TABLET in 1 BOTTLE (71335-2416-4)Marketed from Nov 12, 2024
71335-2416-57133524160520 TABLET in 1 BOTTLE (71335-2416-5)Marketed from Nov 12, 2024
71335-2416-67133524160690 TABLET in 1 BOTTLE (71335-2416-6)Marketed from Nov 12, 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)
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 204467
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2416_670aae9c-2d5a-49f9-996f-def0e9dbff64SPL ID 670aae9c-2d5a-49f9-996f-def0e9dbff64SPL set ID b943dbb1-7f54-434c-9439-8ce768d94ff4RxCUI 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

N471335241601 followed by a unit qualifier and the quantity

Package 71335-2416-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Allopurinol Tablets are indicated for: The management of adults with signs and symptoms of primary or secondary gout (acute attacks, tophi, joint destruction, uric acid lithiasis, and/or nephropathy) The management of adult and pediatric patients with leukemia, lymphoma and solid tumor malignancies who are receiving cancer therapy which causes elevations of serum and urinary uric acid levels The management of adult patients with recurrent calcium oxalate calculi whose daily uric acid excretion exceeds 800 mg/day in male patients and 750 mg/day in female patients, despite lifestyle changes (such as reduction of dietary sodium, non-dairy animal protein, oxylate rich foods, refined sugars and i…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204467

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

FDA NDC Directory listings under ANDA 204467
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-694
AllopurinolAllopurinol 300 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-722
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-4693
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-6715
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-6716
AllopurinolAllopurinol 300 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3605
AllopurinolAllopurinol 300 mg/1TabletOralDirect_Rx72189-417
AllopurinolAllopurinol 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3871
AllopurinolAllopurinol 100 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-693
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack71335-3154
AllopurinolAllopurinol 100 mg/1TabletOralIndoco Remedies Limited14445-170
AllopurinolAllopurinol 300 mg/1TabletOralIndoco Remedies Limited14445-171
AllopurinolAllopurinol 200 mg/1TabletOralIndoco Remedies Limited14445-172
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-4556
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack71335-9634
AllopurinolAllopurinol 300 mg/1TabletOralA-S Medication Solutions50090-6882
AllopurinolAllopurinol 100 mg/1TabletOralREMEDYREPACK INC.70518-4062
AllopurinolAllopurinol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8337
AllopurinolAllopurinol 100 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-240
AllopurinolAllopurinol 200 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-241

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