Allopurinol NDC 53489-156

NDC codes

FDA NDC Directory

Product NDC (as listed)53489-156Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53489-0156Add 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 NDC	11-digit (billing)	Package
53489-156-01	53489015601	100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01)Marketed from Jan 9, 1987
53489-156-02	53489015602	50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02)Marketed from Jan 9, 1987
53489-156-05	53489015605	500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05)Marketed from Jan 9, 1987
53489-156-10	53489015610	1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10)Marketed from Jan 9, 1987

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
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071450
Marketing start: Jan 9, 1987
Listing expires: Dec 31, 2027
Other FDA classes: Xanthine Oxidase Inhibitors (Mechanism)
Identifiers: Product ID 53489-156_57e38626-7a9d-4140-e063-6294a90acd2eSPL ID 57e38626-7a9d-4140-e063-6294a90acd2eSPL set ID fd8f8b8b-f25e-46e9-969a-65363b66e09bRxCUI 197319, 197320UNII 63CZ7GJN5IUPC 0353489156011, 0353489157018
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

N453489015601 followed by a unit qualifier and the quantity

Package 53489-0156-01. 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 Jul 31, 2026.

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 oxylate 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, oxalate 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 071450

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

FDA NDC Directory listings under ANDA 071450
Product	Strength	Form · route	Labeler	Product NDC
Allopurinol	Allopurinol 300 mg/1	TabletOral	Northwind Health Company, LLC	51655-968
Allopurinol	Allopurinol 100 mg/1	TabletOral	Northwind Health Company, LLC	51655-082
Allopurinol	Allopurinol 300 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	53489-157
Allopurinol	Allopurinol 300 mg/1	TabletOral	Proficient Rx LP	71205-377
Allopurinol	Allopurinol 300 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-934
Allopurinol	Allopurinol 100 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-935
Allopurinol	Allopurinol 100 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-975
Allopurinol	Allopurinol 300 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-976
Allopurinol	Allopurinol 100 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-197
Allopurinol	Allopurinol 300 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-253
Allopurinol	Allopurinol 100 mg/1	TabletOral	Bryant Ranch Prepack	71335-2775
Allopurinol	Allopurinol 100 mg/1	TabletOral	Proficient Rx LP	71205-208