NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2079Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2079Add 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
67296-2079-2672962079026729620790220 TABLET, FILM COATED in 1 BOTTLE (67296-2079-2)Marketed from Mar 29, 2006

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)
Cefuroxime Axetil
Generic name (nonproprietary)
cefuroxime axetil
Active ingredients
Cefuroxime axetil — 500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Redpharm DrugNDC labeler code 67296
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065308
Marketing start
Listing expires
Other FDA classes
Cephalosporins (Chemical structure)
Identifiers
Product ID 67296-2079_5b2e7ec0-7c69-4d62-e063-6294a90a7bd5SPL ID 5b2e7ec0-7c69-4d62-e063-6294a90a7bd5
Pharmacologic class
Cephalosporin Antibacterial

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

N467296207902 followed by a unit qualifier and the quantity

Package 67296-2079-02. 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.

About NDC 67296-2079

What is NDC 67296-2079?
67296-2079 is the product NDC for Cefuroxime Axetil, Cefuroxime axetil 500 mg/1 tablet, film coated, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cefuroxime Axetil.
What is the active ingredient?
Cefuroxime axetil.
Who is the labeler?
Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cefuroxime Axetil?
40 other product NDCs are listed under this name. See all Cefuroxime Axetil 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 Cefuroxime Axetil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cefuroxime axetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-057180425-0571-0180425-0571-02
Cefuroxime axetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-754200904-7542-10
Cefuroxime AxetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-890568788-8905-02
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralCoupler LLC67046-130767046-1307-03
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralCoupler LLC67046-108167046-1081-03
Cefuroxime axetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-28360687-0283-94
Cefuroxime AxetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-321570518-3215-04
Cefuroxime axetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-27260687-0272-94
Cefuroxime axetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-65643063-0656-1443063-0656-20
Cefuroxime axetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-65743063-0657-2043063-0657-60

All 41 Cefuroxime Axetil NDCs

Other NDCs under ANDA 065308

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

FDA NDC Directory listings under ANDA 065308
ProductStrengthForm · routeLabelerProduct NDC
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralNorthStar Rx LLC16714-400
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralNorthStar Rx LLC16714-401
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-623
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralA-S Medication Solutions50090-0781
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralA-S Medication Solutions50090-0782
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralA-S Medication Solutions50090-4153
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralA-S Medication Solutions50090-6999
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralA-S Medication Solutions50090-7095
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralA-S Medication Solutions50090-7667
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralA-S Medication Solutions50090-7668
Cefuroxime AxetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.57237-058
Cefuroxime AxetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.57237-059
Cefuroxime AxetilCefuroxime axetil 125 mg/1TabletOralAurobindo Pharma Limited65862-698
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralAurobindo Pharma Limited65862-699
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralAurobindo Pharma Limited65862-700
Cefuroxime AxetilCefuroxime axetil 500 mg/1TabletOralCoupler LLC67046-1081
Cefuroxime AxetilCefuroxime axetil 250 mg/1TabletOralCoupler LLC67046-1307
Cefuroxime AxetilCefuroxime axetil 250 mg/1Tablet, Film coatedOralRedpharm Drug67296-2265
Cefuroxime AxetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3899
Cefuroxime AxetilCefuroxime axetil 500 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8905

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