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Esomeprazole sodium

NDC 70436-190, Esomeprazole sodium, injection, powder, lyophilized, for solution, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-190
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215732
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESOMEPRAZOLE SODIUM40 mg/5mL

Pharmacologic classes

Cytochrome P450 2C19 Inhibitors [MoA]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
70436-190-827043601908210 VIAL in 1 CARTON (70436-190-82) / 5 mL in 1 VIAL (70436-190-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/23395673-116d-4a8e-b0ce-59f9ca5b3daf

Use it

Look up 70436-190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-190. 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.