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droxidopa

NDC 63304-112, droxidopa, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-112
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214384
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DROXIDOPA300 ug/1

Pharmacologic classes

Catecholamines [CS]; Increased Blood Pressure [PE]

Package NDCNDC-11Package
63304-112-906330401129090 CAPSULE in 1 BOTTLE (63304-112-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51ef3096-4622-4f45-a180-ab0dc6d46df9

Use it

Look up 63304-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-112. 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.