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IBUPAK

NDC 59088-756, Ibuprofen, kit, from PureTek Corporation.

Product NDC
59088-756
Status
Listed
Labeler
PureTek Corporation
Dosage form
KIT
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-756 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
59088-756-00590880756001 KIT in 1 KIT (59088-756-00) * 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a63f3857-92d1-0adf-e053-2995a90a3afa

Use it

Look up 59088-756 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-756 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-756. 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.