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Midodrine Hydrochloride

NDC 71205-904, midodrine hydrochloride, tablet, from Proficient Rx LP.

Product NDC
71205-904
Status
Listed
Labeler
Proficient Rx LP
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/71205-904 \
  -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
71205-904-0071205090400100 TABLET in 1 BOTTLE, PLASTIC (71205-904-00)
71205-904-11712050904111000 TABLET in 1 BOTTLE, PLASTIC (71205-904-11)
71205-904-307120509043030 TABLET in 1 BOTTLE, PLASTIC (71205-904-30)
71205-904-5571205090455500 TABLET in 1 BOTTLE, PLASTIC (71205-904-55)
71205-904-607120509046060 TABLET in 1 BOTTLE, PLASTIC (71205-904-60)
71205-904-7271205090472120 TABLET in 1 BOTTLE, PLASTIC (71205-904-72)
71205-904-907120509049090 TABLET in 1 BOTTLE, PLASTIC (71205-904-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0aebf5f9-8cfa-4b77-ba40-821ce0a2b266

Use it

Look up 71205-904 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-904 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-904. 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.