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Hydralazine Hydrochloride

NDC 50228-184, Hydralazine Hydrochloride, tablet, from ScieGen Pharmaceuticals, Inc..

Product NDC
50228-184
Status
Listed
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205236
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-184 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDRALAZINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
50228-184-0150228018401100 TABLET in 1 BOTTLE (50228-184-01)
50228-184-10502280184101000 TABLET in 1 BOTTLE (50228-184-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/500b7f76-5f4e-4e7d-85c3-18b9f66d7504

  • NADAC price for package 50228018401

    GET /v1/drugs/nadac/50228018401

  • NADAC price for package 50228018410

    GET /v1/drugs/nadac/50228018410

Use it

Look up 50228-184 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-184 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-184. 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.