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Ephedrine Sulfate

NDC 25021-836, Ephedrine Sulfate, injection, solution, from Sagent Pharmaceuticals.

Product NDC
25021-836
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214528
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EPHEDRINE SULFATE50 mg/mL

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Increased Norepinephrine Activity [PE]; Norepinephrine Releasing Agent [EPC]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
25021-836-012502108360125 VIAL in 1 CARTON (25021-836-01) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/614e6649-a0e1-4428-855b-363abdb126d8

Use it

Look up 25021-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-836. 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.