What is NDC 67046-0681?

67046-0681 is the product NDC for Allopurinol, Allopurinol 300 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Coupler LLC, NDC labeler code 67046. 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 67046-0681 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67046-0681Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67046-0681Add 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	Copy
67046-0681-3	6704606810367046068103	30 TABLET in 1 BLISTER PACK (67046-0681-3)Marketed from Feb 23, 2018

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 — 300 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Coupler LLCNDC labeler code 67046
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 018659
Marketing start: Feb 23, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Xanthine Oxidase Inhibitors (Mechanism)
Identifiers: Product ID 67046-0681_6a275cd1-052a-1312-e053-2991aa0a9ee0SPL ID 6a275cd1-052a-1312-e053-2991aa0a9ee0SPL set ID 65171cf0-8486-1ca6-e053-2991aa0ab91fRxCUI 197320UNII 63CZ7GJN5IUPC 0303780181052
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

N467046068103 followed by a unit qualifier and the quantity

Package 67046-0681-03. 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 Apr 18, 2018.

Full label on DailyMed (opens in a new tab)

About NDC 67046-0681

What is NDC 67046-0681?: 67046-0681 is the product NDC for Allopurinol, Allopurinol 300 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, 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?: Coupler LLC, NDC labeler code 67046. 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 018659

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

FDA NDC Directory listings under ANDA 018659
Product	Strength	Form · route	Labeler	Product NDC
Allopurinol	Allopurinol 100 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0137
Allopurinol	Allopurinol 300 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0181
Allopurinol	Allopurinol 300 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	43353-186
Allopurinol	Allopurinol 100 mg/1	TabletOral	Safecor Health, LLC	48433-002
Allopurinol	Allopurinol 300 mg/1	TabletOral	Safecor Health, LLC	48433-003
Allopurinol	Allopurinol 100 mg/1	TabletOral	Mylan Institutional Inc.	51079-205
Allopurinol	Allopurinol 300 mg/1	TabletOral	Mylan Institutional Inc.	51079-206
Allopurinol	Allopurinol 300 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0282
Allopurinol	Allopurinol 300 mg/1	TabletOral	Cardinal Health 107, LLC	55154-5454
Allopurinol	Allopurinol 100 mg/1	TabletOral	Cardinal Health 107, LLC	55154-5534
Allopurinol	Allopurinol 100 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	67544-736
Allopurinol	Allopurinol 300 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8424
Allopurinol	Allopurinol 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4412
Allopurinol	Allopurinol 300 mg/1	TabletOral	Bryant Ranch Prepack	71335-9676
Allopurinol	Allopurinol 300 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0383