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NDC 82111-201, buprenorphine hydrochloride and naloxone hydrochloride, tablet, orally disintegrating, from Edenbridge Pharmaceuticals LLC..

Product NDC
82111-201
Status
Listed
Labeler
Edenbridge Pharmaceuticals LLC.
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204242
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82111-201 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE.7 mg/1
  • NALOXONE HYDROCHLORIDE.18 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82111-201-30821110201303 BLISTER PACK in 1 CARTON (82111-201-30) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/57583c1d-9c44-4503-917d-68dba7377bd1

  • NADAC price for package 82111020130

    GET /v1/drugs/nadac/82111020130

Use it

Look up 82111-201 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82111-201 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82111-201. 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.