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Nalbuphine hydrochloride

NDC 70069-662, Nalbuphine hydrochloride, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-662
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216049
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-662 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALBUPHINE HYDROCHLORIDE20 mg/mL

Pharmacologic classes

Competitive Opioid Antagonists [MoA]; Opioid Agonist/Antagonist [EPC]; Partial Opioid Agonists [MoA]

Package NDCNDC-11Package
70069-662-10700690662101 VIAL, MULTI-DOSE in 1 CARTON (70069-662-10) / 10 mL in 1 VIAL, MULTI-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d82dafac-cce7-445a-8127-2a10b6d947ca

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-662

Use it

Look up 70069-662 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-662 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-662. 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.