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Cefpodoxime Proxetil

NDC 0781-5439, Cefpodoxime Proxetil, tablet, film coated, from Sandoz Inc.

Product NDC
0781-5439
Status
Listed
Labeler
Sandoz Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065462
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-5439 \
  -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
0781-5439-0100781543901100 TABLET, FILM COATED in 1 BOTTLE (0781-5439-01)
0781-5439-200078154392020 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8519a9d8-7106-4545-bc58-859ee9a6708e

  • NADAC price for package 00781543901

    GET /v1/drugs/nadac/00781543901

  • NADAC price for package 00781543920

    GET /v1/drugs/nadac/00781543920

Use it

Look up 0781-5439 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-5439 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-5439. 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.