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NDC 59088-083, sumatriptan succinate, camphor, menthol, kit, from PureTek Corporation.

Product NDC
59088-083
Status
Listed
Labeler
PureTek Corporation
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-083 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
59088-083-00590880083001 KIT in 1 PACKAGE (59088-083-00) * 9 BLISTER PACK in 1 CARTON (55111-292-09) / 9 TABLET in 1 BLISTER PACK * 85 g in 1 BOTTLE, WITH APPLICATOR (59088-283-07)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b82d7d65-9ef4-4f05-9a7d-10440683332e

Use it

Look up 59088-083 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-083 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-083. 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.