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Dobutamine

NDC 70436-203, dobutamine, injection, from Slate Run Pharmaceuticals.

Product NDC
70436-203
Status
Listed
Labeler
Slate Run Pharmaceuticals
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216131
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-203 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOBUTAMINE HYDROCHLORIDE250 mg/20mL

Pharmacologic classes

Adrenergic beta-Agonists [MoA]; beta-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
70436-203-80704360203801 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-80) / 20 mL in 1 VIAL, SINGLE-DOSE
70436-203-827043602038210 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-82) / 20 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ee09a55f-9992-48bb-b8d6-1184bd548536

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70436-203

Use it

Look up 70436-203 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-203 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-203. 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.