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Cefpodoxime Proxetil

NDC 67877-879, Cefpodoxime Proxetil, tablet, film coated, from Ascend Laboratories, LLC.

Product NDC
67877-879
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210568
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-879 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFPODOXIME PROXETIL200 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
67877-879-0167877087901100 TABLET, FILM COATED in 1 BOTTLE (67877-879-01)
67877-879-0567877087905500 TABLET, FILM COATED in 1 BOTTLE (67877-879-05)
67877-879-206787708792020 TABLET, FILM COATED in 1 BOTTLE (67877-879-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce5646cb-a450-4c2c-8499-6ecf71b12b0e

  • NADAC price for package 67877087920

    GET /v1/drugs/nadac/67877087920

Use it

Look up 67877-879 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-879 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-879. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.