NDC codes

FDA NDC Directory
Product NDC (as listed)71205-377Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0377Add 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
71205-377-307120503773030 TABLET in 1 BOTTLE, PLASTIC (71205-377-30)Marketed from Dec 26, 2019
71205-377-607120503776060 TABLET in 1 BOTTLE, PLASTIC (71205-377-60)Marketed from Dec 26, 2019
71205-377-907120503779090 TABLET in 1 BOTTLE, PLASTIC (71205-377-90)Marketed from Dec 26, 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 — 300 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
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 71205-377_220da8f7-55dd-4b01-8dad-bb756856202aSPL ID 220da8f7-55dd-4b01-8dad-bb756856202aSPL set ID b20c6ed4-6b94-4a1b-b448-e910856fa825RxCUI 197320UNII 63CZ7GJN5IUPC 0371205377908
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

N471205037730 followed by a unit qualifier and the quantity

Package 71205-0377-30. 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.

About NDC 71205-377

What is NDC 71205-377?
71205-377 is the product NDC for Allopurinol, Allopurinol 300 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Allopurinol.
What is the active ingredient?
Allopurinol.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allopurinol?
167 other product NDCs are listed under this name. See all Allopurinol NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Allopurinol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AllopurinolAllopurinol 300 mg/1TabletOralCardinal Health 107, LLC55154-028255154-0282-00
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-469370518-4693-00
AllopurinolAllopurinol 100 mg/1TabletOralSafecor Health, LLC48433-00248433-0002-20
AllopurinolAllopurinol 300 mg/1TabletOralSafecor Health, LLC48433-00348433-0003-20
AllopurinolAllopurinol 300 mg/1TabletOralCoupler LLC67046-165867046-1658-03
AllopurinolAllopurinol 300 mg/1TabletOralREMEDYREPACK INC.70518-455670518-4556-00
AllopurinolAllopurinol 300 mg/1TabletOralNorthwind Health Company, LLC82868-09982868-0099-3082868-0099-90
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-01953401-0019-6053401-0019-80
AllopurinolAllopurinol 300 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-02553401-0025-60
AllopurinolAllopurinol 100 mg/1TabletOralXLCare Pharmaceuticals Inc.72865-30372865-0303-0172865-0303-0572865-0303-10+1 more

All 168 Allopurinol NDCs

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/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/1TabletOralNorthwind Health Company, LLC51655-082
AllopurinolAllopurinol 300 mg/1TabletOralNorthwind Health Company, LLC51655-968
AllopurinolAllopurinol 100 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-156
AllopurinolAllopurinol 300 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-157
AllopurinolAllopurinol 100 mg/1TabletOralProficient Rx LP71205-208
AllopurinolAllopurinol 100 mg/1TabletOralBryant Ranch Prepack71335-2775
AllopurinolAllopurinol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-197
AllopurinolAllopurinol 300 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-253

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