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Midodrine Hydrochloride

NDC 71335-3037, Midodrine Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3037
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212774
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3037 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIDODRINE HYDROCHLORIDE2.5 mg/1

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
71335-3037-171335303701100 TABLET in 1 BOTTLE (71335-3037-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/78d447cb-e3ff-433b-9758-b907a75b0666

Use it

Look up 71335-3037 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3037 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3037. 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.