NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8517Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8517Add 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
0615-8517-050061585170515 TABLET in 1 BLISTER PACK (0615-8517-05)Marketed from Aug 13, 2024
0615-8517-390061585173930 TABLET in 1 BLISTER PACK (0615-8517-39)Marketed from Aug 13, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 300 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075798
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 0615-8517_15f23e0f-50fc-4ac9-8f68-c0b453eda0c9SPL ID 15f23e0f-50fc-4ac9-8f68-c0b453eda0c9SPL set ID 1da7d9d4-ed94-4fe6-827a-6f4b3bdce3c3RxCUI 197319, 197320UNII 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

N400615851705 followed by a unit qualifier and the quantity

Package 00615-8517-05. 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 075798

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

FDA NDC Directory listings under ANDA 075798
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralCardinal Health 107, LLC55154-7981
AllopurinolAllopurinol 300 mg/1TabletOralMajor Pharmaceuticals0904-6572
AllopurinolAllopurinol 300 mg/1TabletOralPar Health USA, LLC0603-2116
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-4286
AllopurinolAllopurinol 100 mg/1TabletOralPar Health USA, LLC0603-2115
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack72162-1149
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack72162-1150
AllopurinolAllopurinol 100 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8385
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack63629-2111
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack63629-2112
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack63629-2113

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Allopurinol NDC 0615-8517 | Med-Code