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EPHEDRINE SULFATE

NDC 70518-4433, EPHEDRINE SULFATE, injection, from REMEDYREPACK INC..

Product NDC
70518-4433
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216146
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4433 \
  -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
70518-4433-07051844330010 VIAL in 1 CARTON (70518-4433-0) / 1 mL in 1 VIAL (70518-4433-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9851cc1c-f267-4e18-b1ad-923fe9cded84

Use it

Look up 70518-4433 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4433 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4433. 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.