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Midodrine Hydrochloride

NDC 0904-7641, Midodrine Hydrochloride, tablet, from Major Pharmaceuticals.

Product NDC
0904-7641
Status
Listed
Labeler
Major Pharmaceuticals
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217271
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7641 \
  -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
0904-7641-06009047641065 BLISTER PACK in 1 CARTON (0904-7641-06) / 10 TABLET in 1 BLISTER PACK (0904-7641-35)
0904-7641-610090476416110 BLISTER PACK in 1 CARTON (0904-7641-61) / 10 TABLET in 1 BLISTER PACK (0904-7641-35)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dccf040b-e8de-40b5-9977-8b3e56830157

Use it

Look up 0904-7641 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7641 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-7641. 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.