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BUPRENORPHINE

NDC 87441-082, BUPRENORPHINE, tablet, from Unit Dose Solutions, Inc..

Product NDC
87441-082
Status
Listed
Labeler
Unit Dose Solutions, Inc.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207276
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87441-082 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE8 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
87441-082-018744100820130 TABLET in 1 BLISTER PACK (87441-082-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5578cd5c-c860-6e8a-e063-6394a90a56c7

Use it

Look up 87441-082 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87441-082 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87441-082. 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.