NDC codes

FDA NDC Directory
Product NDC (as listed)43353-186Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43353-0186Add 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
43353-186-604335301866090 TABLET in 1 BOTTLE (43353-186-60)Marketed from Jun 17, 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 — 300 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 018659
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 43353-186_8b90efb6-87d0-428c-b0ef-13237a009714SPL ID 8b90efb6-87d0-428c-b0ef-13237a009714SPL set ID aea483a7-4ce7-4fe5-936c-fd876b4fa3a8RxCUI 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

N443353018660 followed by a unit qualifier and the quantity

Package 43353-0186-60. 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 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
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralCoupler LLC67046-0681
AllopurinolAllopurinol 300 mg/1TabletOralCardinal Health 107, LLC55154-0282
AllopurinolAllopurinol 100 mg/1TabletOralSafecor Health, LLC48433-002
AllopurinolAllopurinol 300 mg/1TabletOralSafecor Health, LLC48433-003
AllopurinolAllopurinol 300 mg/1TabletOralCardinal Health 107, LLC55154-5454
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack71335-9676
AllopurinolAllopurinol 100 mg/1TabletOralCardinal Health 107, LLC55154-5534
AllopurinolAllopurinol 100 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0137
AllopurinolAllopurinol 300 mg/1TabletOralMylan Institutional Inc.51079-206
AllopurinolAllopurinol 100 mg/1TabletOralMylan Institutional Inc.51079-205
AllopurinolAllopurinol 300 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0181
AllopurinolAllopurinol 300 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0383
AllopurinolAllopurinol 300 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8424
AllopurinolAllopurinol 100 mg/1TabletOralREMEDYREPACK INC.70518-4412
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC67544-736

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