Allopurinol NDC 55154-2338

NDC codes

FDA NDC Directory

Product NDC (as listed)55154-2338Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55154-2338Add 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
55154-2338-0	55154233800	10 BLISTER PACK in 1 BAG (55154-2338-0) / 1 TABLET in 1 BLISTER PACKMarketed from Feb 8, 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 — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cardinal Health 107, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210117
Marketing start: Feb 8, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Xanthine Oxidase Inhibitors (Mechanism)
Identifiers: Product ID 55154-2338_25c55ba6-964c-453d-a1be-0420ddb39139SPL ID 25c55ba6-964c-453d-a1be-0420ddb39139SPL set ID 2462b4b5-8313-4e4d-93ac-839de4a29520RxCUI 197319UNII 63CZ7GJN5IUPC 0055154233804
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

N455154233800 followed by a unit qualifier and the quantity

Package 55154-2338-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 210117

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

FDA NDC Directory listings under ANDA 210117
Product	Strength	Form · route	Labeler	Product NDC
Allopurinol	Allopurinol 200 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-2009
Allopurinol	Allopurinol 100 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1209
Allopurinol	Allopurinol 300 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1210
Allopurinol	Allopurinol 300 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1127
Allopurinol	Allopurinol 100 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1126
Allopurinol	Allopurinol 100 mg/1	TabletOral	Major Pharmaceuticals	0904-7041
Allopurinol	Allopurinol 200 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1907