NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2744Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2744Add 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
71335-2744-171335274401100 TABLET in 1 BOTTLE (71335-2744-1)Marketed from Oct 2, 2025
71335-2744-27133527440230 TABLET in 1 BOTTLE (71335-2744-2)Marketed from Oct 2, 2025
71335-2744-37133527440360 TABLET in 1 BOTTLE (71335-2744-3)Marketed from Oct 2, 2025
71335-2744-471335274404120 TABLET in 1 BOTTLE (71335-2744-4)Marketed from Oct 2, 2025
71335-2744-57133527440520 TABLET in 1 BOTTLE (71335-2744-5)Marketed from Oct 2, 2025
71335-2744-67133527440690 TABLET in 1 BOTTLE (71335-2744-6)Marketed from Oct 2, 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)
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 217748
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2744_17448c5c-7701-4767-91f8-238b570e9921SPL ID 17448c5c-7701-4767-91f8-238b570e9921SPL set ID e453a5e0-44c3-4eb5-a8d0-7c02157d2f8cRxCUI 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

N471335274401 followed by a unit qualifier and the quantity

Package 71335-2744-01. 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…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217748

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

FDA NDC Directory listings under ANDA 217748
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralDirect_Rx72189-647
AllopurinolAllopurinol 300 mg/1TabletOralA-S Medication Solutions50090-7351
AllopurinolAllopurinol 300 mg/1TabletOralA-S Medication Solutions50090-7353
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-7696
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-7697
AllopurinolAllopurinol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4027
AllopurinolAllopurinol 300 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0518
AllopurinolAllopurinol 300 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8865
AllopurinolAllopurinol 100 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-252
AllopurinolAllopurinol 300 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-253
AllopurinolAllopurinol 300 mg/1TabletOralNorthwind Health Company, LLC82868-099
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-7791
AllopurinolAllopurinol 300 mg/1TabletOralA-S Medication Solutions50090-7792
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-4404
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-019
AllopurinolAllopurinol 100 mg/1TabletOralXLCare Pharmaceuticals Inc.72865-303
AllopurinolAllopurinol 300 mg/1TabletOralXLCare Pharmaceuticals Inc.72865-304
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack71335-3082
AllopurinolAllopurinol 300 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-025

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