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Midodrine Hydrochloride

NDC 70700-158, midodrine hydrochloride, tablet, from Xiromed, LLC.

Product NDC
70700-158
Status
Listed
Labeler
Xiromed, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207849
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70700-158 \
  -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
70700-158-0170700015801100 TABLET in 1 BOTTLE, PLASTIC (70700-158-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4332a41-2a0a-a14a-9ce5-1465f39ff725

  • NADAC price for package 70700015801

    GET /v1/drugs/nadac/70700015801

Use it

Look up 70700-158 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70700-158 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70700-158. 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.