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Cefprozil

NDC 65862-069, Cefprozil, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-069
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065340
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-069 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFPROZIL500 mg/1
Package NDCNDC-11Package
65862-069-0165862006901100 TABLET, FILM COATED in 1 BOTTLE (65862-069-01)
65862-069-0565862006905500 TABLET, FILM COATED in 1 BOTTLE (65862-069-05)
65862-069-306586200693030 TABLET, FILM COATED in 1 BOTTLE (65862-069-30)
65862-069-506586200695050 TABLET, FILM COATED in 1 BOTTLE (65862-069-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b9111a81-07c4-4458-b994-a4ad504986d8

  • NADAC price for package 65862006901

    GET /v1/drugs/nadac/65862006901

Use it

Look up 65862-069 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-069 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-069. 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.