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Buprenorphine Sublingual C-III

NDC 72189-582, Buprenorphine Sublingual C-III, tablet, from Direct_Rx.

Product NDC
72189-582
Status
Listed
Labeler
Direct_Rx
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078633
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-582 \
  -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
72189-582-607218905826060 TABLET in 1 BOTTLE (72189-582-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/248524c6-4c8b-a450-e063-6394a90a81ef

Use it

Look up 72189-582 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-582 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-582. 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.