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Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate

NDC 87441-003, Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate, tablet, from Unit Dose Solutions, Inc..

Product NDC
87441-003
Status
Listed
Labeler
Unit Dose Solutions, Inc.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207000
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87441-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE2 mg/1
  • NALOXONE HYDROCHLORIDE DIHYDRATE.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
87441-003-018744100030130 TABLET in 1 BLISTER PACK (87441-003-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4f979409-f9a2-d3a2-e063-6394a90accd0

Use it

Look up 87441-003 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87441-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87441-003. 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.