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Folixate

NDC 59088-301, Folate, Vitamin D3, tablet, from PureTek Corporation.

Product NDC
59088-301
Status
Listed
Labeler
PureTek Corporation
Dosage form
TABLET
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/59088-301 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOMEFOLATE CALCIUM1000 ug/1
  • VITAMIN D125 ug/1

Pharmacologic classes

Folate Analog [EPC]; Folic Acid [CS]; Vitamin D [CS]; Vitamin D [EPC]

Package NDCNDC-11Package
59088-301-545908803015430 TABLET in 1 BOTTLE, PLASTIC (59088-301-54)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0bb91f61-b61b-c894-e063-6394a90ae51c

Use it

Look up 59088-301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-301. 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.