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Droxidopa

NDC 70710-1390, Droxidopa, capsule, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1390
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211818
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1390 \
  -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
70710-1390-97071013900990 CAPSULE in 1 BOTTLE (70710-1390-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aa3ce55a-1ea9-4b50-b682-6f25398bcc29

  • NADAC price for package 70710139009

    GET /v1/drugs/nadac/70710139009

Use it

Look up 70710-1390 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1390 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1390. 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.