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Isoproterenol Hydrochloride

NDC 69918-735, Isoproterenol Hydrochloride, injection, solution, from Nordic Pharma, Inc..

Product NDC
69918-735
Status
Listed
Labeler
Nordic Pharma, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRACARDIAC, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211237
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69918-735 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ISOPROTERENOL HYDROCHLORIDE.2 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
69918-735-106991807351010 VIAL, SINGLE-DOSE in 1 CARTON (69918-735-10) / 5 mL in 1 VIAL, SINGLE-DOSE
69918-735-116991807351110 VIAL, SINGLE-DOSE in 1 CARTON (69918-735-11) / 5 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=69918-735

Use it

Look up 69918-735 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69918-735 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69918-735. 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.