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EPHEDRINE SULFATE

NDC 70069-819, EPHEDRINE SULFATE, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-819
Status
Listed
Labeler
Somerset Therapeutics, LLC
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/70069-819 \
  -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
70069-819-107006908191010 VIAL in 1 CARTON (70069-819-10) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/86b1c42c-854e-463b-ac99-4aacbbe71fd1

Use it

Look up 70069-819 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-819 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-819. 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.