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Ephedrine Sulfate

NDC 0781-3269, Ephedrine Sulfate, injection, from Sandoz Inc.

Product NDC
0781-3269
Status
Listed
Labeler
Sandoz Inc
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209784
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3269 \
  -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
0781-3269-950078132699510 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c8af7bb5-41da-4f8c-8acd-f489892a0d72

Use it

Look up 0781-3269 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3269 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-3269. 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.