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Buprenorphine Sublingual

NDC 72189-579, Buprenorphine Sublingual, tablet, from Direct_rx.

Product NDC
72189-579
Status
Listed
Labeler
Direct_rx
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201760
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-579 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72189-579-607218905796060 TABLET in 1 BOTTLE (72189-579-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2204e135-6a0c-68a2-e063-6394a90ac019

Use it

Look up 72189-579 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-579 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-579. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.