NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2331Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2331Add 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
67296-2331-1672962331016729623310110 TABLET, FILM COATED in 1 BOTTLE (67296-2331-1)Marketed from Mar 1, 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)
Cefpodoxime Proxetil
Generic name (nonproprietary)
cefpodoxime proxetil
Active ingredients
Cefpodoxime proxetil — 100 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 210568
Marketing start
Listing expires
Other FDA classes
Cephalosporins (Chemical structure)
Identifiers
Product ID 67296-2331_5b42e3a1-940a-28ab-e063-6294a90a02baSPL ID 5b42e3a1-940a-28ab-e063-6294a90a02ba
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

N467296233101 followed by a unit qualifier and the quantity

Package 67296-2331-01. 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 67296-2331

What is NDC 67296-2331?
67296-2331 is the product NDC for Cefpodoxime Proxetil, Cefpodoxime proxetil 100 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?
Cefpodoxime Proxetil.
What is the active ingredient?
Cefpodoxime proxetil.
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 Cefpodoxime Proxetil?
26 other product NDCs are listed under this name. See all Cefpodoxime Proxetil 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 Cefpodoxime Proxetil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-467670518-4676-00
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-87867877-0878-0167877-0878-0567877-0878-20
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-361668071-3616-04
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralRedpharm Drug67296-233267296-2332-03
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-87967877-0879-0167877-0879-0567877-0879-20
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-344168071-3441-02
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAmici Pharmaceuticals, LLC.69292-51469292-0514-0169292-0514-50
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAmici Pharmaceuticals, LLC.69292-51669292-0516-0169292-0516-50
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-55967877-0559-0167877-0559-0567877-0559-20
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-56067877-0560-0167877-0560-0567877-0560-20

All 27 Cefpodoxime Proxetil NDCs

Other NDCs under ANDA 210568

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

FDA NDC Directory listings under ANDA 210568
ProductStrengthForm · routeLabelerProduct NDC
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3441
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-559
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAmici Pharmaceuticals, LLC.69292-514
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-560
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAmici Pharmaceuticals, LLC.69292-516
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralRedpharm Drug67296-2332
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4676
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3616
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-084
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-083
Cefpodoxime ProxetilCefpodoxime proxetil 100 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-878
Cefpodoxime ProxetilCefpodoxime proxetil 200 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-879

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