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Midodrine Hydrochloride

NDC 85293-006, Midodrine Hydrochloride, tablet, from Umasuto, LLC.

Product NDC
85293-006
Status
Listed
Labeler
Umasuto, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207613
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85293-006 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIDODRINE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
85293-006-0185293000601100 TABLET in 1 BOTTLE (85293-006-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4f5e1689-9691-471b-a39c-26120d6ce073

Use it

Look up 85293-006 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85293-006 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85293-006. 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.