NDC codes

FDA NDC Directory
Product NDC (as listed)69315-409Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69315-0409Add 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
69315-409-096931504090990 TABLET in 1 BOTTLE (69315-409-09)Marketed from Sep 1, 2024

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 — 200 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214443
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 69315-409_227ef709-80a3-45e9-807a-2db8abee3a50SPL ID 227ef709-80a3-45e9-807a-2db8abee3a50
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

N469315040909 followed by a unit qualifier and the quantity

Package 69315-0409-09. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 214443

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

FDA NDC Directory listings under ANDA 214443
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralHarman Finochem Limited82638-113
AllopurinolAllopurinol 100 mg/1TabletOralHarman Finochem Limited82638-112
AllopurinolAllopurinol 100 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-710
AllopurinolAllopurinol 100 mg/1TabletOralLeading Pharma, LLC69315-291
AllopurinolAllopurinol 300 mg/1TabletOralLeading Pharma, LLC69315-292
AllopurinolAllopurinol 300 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3672
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack71335-2542
AllopurinolAllopurinol 300 mg/1TabletOralCoupler LLC67046-1639
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-949
AllopurinolAllopurinol 300 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8713
AllopurinolAllopurinol 100 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3803
AllopurinolAllopurinol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8727

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Allopurinol NDC 69315-409 | Med-Code