What is NDC 66267-665?

66267-665 is the product NDC for Allopurinol, Allopurinol 100 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals, Inc., NDC labeler code 66267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Allopurinol?

172 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Allopurinol NDC 66267-665 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)66267-665Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66267-0665Add 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
66267-665-30	6626706653066267066530	30 TABLET in 1 BOTTLE (66267-665-30)Marketed from Dec 28, 2016
66267-665-60	6626706656066267066560	60 TABLET in 1 BOTTLE (66267-665-60)Marketed from Dec 28, 2016
66267-665-90	6626706659066267066590	90 TABLET in 1 BOTTLE (66267-665-90)Marketed from Dec 28, 2016

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: NuCare Pharmaceuticals, Inc.NDC labeler code 66267
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203154
Marketing start: Apr 29, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Xanthine Oxidase Inhibitors (Mechanism)
Identifiers: Product ID 66267-665_1fa77d0a-40f1-b54e-e063-6294a90a0375SPL ID 1fa77d0a-40f1-b54e-e063-6294a90a0375SPL set ID 44bcc8df-a803-010f-e054-00144ff88e88RxCUI 197319UNII 63CZ7GJN5IUPC 0366267665902
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

N466267066530 followed by a unit qualifier and the quantity

Package 66267-0665-30. 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 Aug 14, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE THIS IS NOT AN INNOCUOUS DRUG. IT IS NOT RECOMMENDED FOR THE TREATMENT OF ASYMPTOMATIC HYPERURICEMIA. Allopurinol tablets USP reduces serum and urinary uric acid concentrations. Its use should be individualized for each patient and requires an understanding of its mode of action and pharmacokinetics (see CLINICAL PHARMACOLOGY , CONTRAINDICATIONS , WARNINGS , and PRECAUTIONS ). Allopurinol tablet USP is indicated in: the management of patients with signs and symptoms of primary or secondary gout (acute attacks, tophi, joint destruction, uric acid lithiasis, and/or nephropathy). the management of patients with leukemia, lymphoma and malignancies who are receiving cancer t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66267-665

What is NDC 66267-665?: 66267-665 is the product NDC for Allopurinol, Allopurinol 100 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Allopurinol.
What is the active ingredient?: Allopurinol.
Who is the labeler?: NuCare Pharmaceuticals, Inc., NDC labeler code 66267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allopurinol?: 172 other product NDCs are listed under this name. See all Allopurinol NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Allopurinol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Allopurinol	Allopurinol 100 mg/1	TabletOral	AvPAK	50268-030	50268-0030-10
Allopurinol	Allopurinol 300 mg/1	TabletOral	AvPAK	50268-031	50268-0031-10
Allopurinol	Allopurinol 300 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0282	55154-0282-00
Allopurinol	Allopurinol 300 mg/1	TabletOral	REMEDYREPACK INC.	70518-4693	70518-4693-00
Allopurinol	Allopurinol 300 mg/1	TabletOral	Safecor Health, LLC	48433-003	48433-0003-20
Allopurinol	Allopurinol 100 mg/1	TabletOral	Safecor Health, LLC	48433-002	48433-0002-20
Allopurinol	Allopurinol 300 mg/1	TabletOral	Coupler LLC	67046-1658	67046-1658-03
Allopurinol	Allopurinol 300 mg/1	TabletOral	REMEDYREPACK INC.	70518-4556	70518-4556-00
Allopurinol	Allopurinol 300 mg/1	TabletOral	Northwind Health Company, LLC	82868-099	82868-0099-3082868-0099-90
Allopurinol	Allopurinol 100 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-019	53401-0019-6053401-0019-80

All 173 Allopurinol NDCs

Other NDCs under ANDA 203154

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

FDA NDC Directory listings under ANDA 203154
Product	Strength	Form · route	Labeler	Product NDC
Allopurinol	Allopurinol 100 mg/1	TabletOral	Accord Healthcare Inc.	16729-134
Allopurinol	Allopurinol 300 mg/1	TabletOral	Accord Healthcare Inc.	16729-135
Allopurinol	Allopurinol 100 mg/1	TabletOral	A-S Medication Solutions	50090-5168
Allopurinol	Allopurinol 100 mg/1	TabletOral	Northwind Health Company, LLC	51655-523
Allopurinol	Allopurinol 300 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-6323
Allopurinol	Allopurinol 300 mg/1	TabletOral	Proficient Rx LP	71205-049
Allopurinol	Allopurinol 300 mg/1	TabletOral	Bryant Ranch Prepack	71335-0112
Allopurinol	Allopurinol 100 mg/1	TabletOral	Bryant Ranch Prepack	71335-0467
Allopurinol	Allopurinol 100 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-678
Allopurinol	Allopurinol 300 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0206