NDC codes

FDA NDC Directory
Product NDC (as listed)71205-208Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0208Add 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
71205-208-307120502083030 TABLET in 1 BOTTLE, PLASTIC (71205-208-30)Marketed from Jan 22, 2019
71205-208-607120502086060 TABLET in 1 BOTTLE, PLASTIC (71205-208-60)Marketed from Jan 22, 2019
71205-208-907120502089090 TABLET in 1 BOTTLE, PLASTIC (71205-208-90)Marketed from Jan 22, 2019

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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071450
Marketing start
Listing expires
Other FDA classes
Xanthine Oxidase Inhibitors (Mechanism)
Identifiers
Product ID 71205-208_5fb68d12-481a-45d4-8fed-1a1acb88f665SPL ID 5fb68d12-481a-45d4-8fed-1a1acb88f665SPL set ID 06cf0f4b-aef0-472e-b5c0-56e0c35354f2RxCUI 197319UNII 63CZ7GJN5IUPC 0371205208301
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

N471205020830 followed by a unit qualifier and the quantity

Package 71205-0208-30. 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 071450

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

FDA NDC Directory listings under ANDA 071450
ProductStrengthForm · routeLabelerProduct NDC
AllopurinolAllopurinol 300 mg/1TabletOralNorthwind Health Company, LLC51655-968
AllopurinolAllopurinol 100 mg/1TabletOralNorthwind Health Company, LLC51655-082
AllopurinolAllopurinol 300 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-157
AllopurinolAllopurinol 100 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-156
AllopurinolAllopurinol 300 mg/1TabletOralProficient Rx LP71205-377
AllopurinolAllopurinol 300 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-934
AllopurinolAllopurinol 100 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-935
AllopurinolAllopurinol 100 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-975
AllopurinolAllopurinol 300 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-976
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-197
AllopurinolAllopurinol 300 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-253
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack71335-2775

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