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DROXIDOPA

NDC 69452-257, DROXIDOPA, capsule, from Bionpharma Inc..

Product NDC
69452-257
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213033
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-257 \
  -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
69452-257-196945202571990 CAPSULE in 1 BOTTLE, PLASTIC (69452-257-19)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3cfd280-3548-b590-e053-2a95a90a5eb3

Use it

Look up 69452-257 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-257 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-257. 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.