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droxidopa

NDC 70436-141, droxidopa, capsule, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-141
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215265
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-141 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DROXIDOPA200 mg/1

Pharmacologic classes

Catecholamines [CS]; Increased Blood Pressure [PE]

Package NDCNDC-11Package
70436-141-067043601410690 CAPSULE in 1 BOTTLE (70436-141-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/049f997b-1649-467e-bbb9-bdb991b0bc6e

Use it

Look up 70436-141 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-141 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-141. 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.