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HydrALAZINE Hydrochloride

NDC 71205-072, HydrALAZINE Hydrochloride, tablet, from Proficient Rx LP.

Product NDC
71205-072
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200770
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-072 \
  -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
71205-072-307120500723030 TABLET in 1 BOTTLE (71205-072-30)
71205-072-607120500726060 TABLET in 1 BOTTLE (71205-072-60)
71205-072-907120500729090 TABLET in 1 BOTTLE (71205-072-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dfd60a79-2a30-41e6-b000-a144730099a8

Use it

Look up 71205-072 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-072 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-072. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.