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Nalbuphine hydrochloride

NDC 70069-672, Nalbuphine hydrochloride, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-672
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216050
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-672 \
  -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
70069-672-107006906721010 AMPULE in 1 CARTON (70069-672-10) / 1 mL in 1 AMPULE (70069-672-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a3221c05-5822-4ab8-b589-0e3939b91a68

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-672

Use it

Look up 70069-672 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-672 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-672. 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.