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Hydralazine Hydrochloride

NDC 71335-2307, Hydralazine Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2307
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2307 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDRALAZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Package NDCNDC-11Package
71335-2307-17133523070130 TABLET in 1 BOTTLE (71335-2307-1)
71335-2307-27133523070260 TABLET in 1 BOTTLE (71335-2307-2)
71335-2307-37133523070390 TABLET in 1 BOTTLE (71335-2307-3)
71335-2307-471335230704100 TABLET in 1 BOTTLE (71335-2307-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/914d5b62-6f9b-4665-8562-689367c36230

Use it

Look up 71335-2307 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2307 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2307. 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.