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Buprenorphine and Naloxone

NDC 50742-364, buprenorphine and naloxone, film, from INGENUS PHARMACEUTICALS, LLC.

Product NDC
50742-364
Status
Listed
Labeler
INGENUS PHARMACEUTICALS, LLC
Dosage form
FILM
Route
BUCCAL, SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212756
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-364 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE8 mg/1
  • NALOXONE HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50742-364-305074203643030 POUCH in 1 CARTON (50742-364-30) / 1 FILM in 1 POUCH (50742-364-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4951ec29-609b-4836-b0e4-0d9c1d6ae6fe

  • NADAC price for package 50742036430

    GET /v1/drugs/nadac/50742036430

Use it

Look up 50742-364 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-364 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-364. 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.