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Buprenorphine and Naloxone

NDC 31722-480, buprenorphine and naloxone, film, soluble, from Camber Pharmaceuticals, Inc..

Product NDC
31722-480
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
FILM, SOLUBLE
Route
BUCCAL, SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219850
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-480 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE4 mg/1
  • NALOXONE HYDROCHLORIDE1 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
31722-480-303172204803030 POUCH in 1 CARTON (31722-480-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-480-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/221195e4-de08-414c-af08-a611a74789de

Use it

Look up 31722-480 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-480 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-480. 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.