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Buprenorphine HCl and Naloxone HCl

NDC 71335-1514, Buprenorphine and Naloxone, tablet, from Bryant Ranch Prepack.

Product NDC
71335-1514
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203136
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1514 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE2 mg/1
  • NALOXONE HYDROCHLORIDE DIHYDRATE.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-1514-17133515140130 TABLET in 1 BOTTLE (71335-1514-1)
71335-1514-27133515140210 TABLET in 1 BOTTLE (71335-1514-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e82e2d74-33a8-4894-82f6-788fc0f9feec

Use it

Look up 71335-1514 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1514 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1514. 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.