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Buprenorphine and Naloxone

NDC 62756-969, Buprenorphine and Naloxone, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-969
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201633
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-969 \
  -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
62756-969-64627560969643 BLISTER PACK in 1 CARTON (62756-969-64) / 10 TABLET in 1 BLISTER PACK
62756-969-836275609698330 TABLET in 1 BOTTLE (62756-969-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/91b68606-05de-4586-ae31-07e8cc9160cf

  • NADAC price for package 62756096983

    GET /v1/drugs/nadac/62756096983

Use it

Look up 62756-969 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-969 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-969. 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.