NDC codes

FDA NDC Directory
Product NDC (as listed)68071-2997Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-2997Add 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
68071-2997-36807129970330 TABLET in 1 BOTTLE, PLASTIC (68071-2997-3)Marketed from May 5, 2023
68071-2997-96807129970990 TABLET in 1 BOTTLE, PLASTIC (68071-2997-9)Marketed from May 5, 2023

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211820
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 68071-2997_2d53e60e-6f9e-182d-e063-6294a90ab7f0SPL ID 2d53e60e-6f9e-182d-e063-6294a90ab7f0SPL set ID faf55184-6962-d49f-e053-6394a90a152eRxCUI 197319UNII 63CZ7GJN5IUPC 0368071299731
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

N468071299703 followed by a unit qualifier and the quantity

Package 68071-2997-03. 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

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

Other NDCs under ANDA 211820

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

FDA NDC Directory listings under ANDA 211820
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 100 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-656
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-4662
AllopurinolAllopurinol 300 mg/1TabletOralA-S Medication Solutions50090-4663
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack71335-9641
AllopurinolAllopurinol 100 mg/1TabletOralAmerican Health Packaging60687-677
AllopurinolAllopurinol 300 mg/1TabletOralAmerican Health Packaging60687-688
AllopurinolAllopurinol 100 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-349
AllopurinolAllopurinol 300 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-350
AllopurinolAllopurinol 100 mg/1TabletOralDirect_Rx72189-437
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-7832
AllopurinolAllopurinol 100 mg/1TabletOralA-S Medication Solutions50090-7833
AllopurinolAllopurinol 100 mg/1TabletOralREMEDYREPACK INC.70518-3660
AllopurinolAllopurinol 300 mg/1TabletOralBryant Ranch Prepack71335-2332
AllopurinolAllopurinol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8458
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-3704

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