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Buprenorphine

NDC 62756-460, Buprenorphine, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-460
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201760
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-460 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE8 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62756-460-64627560460643 BLISTER PACK in 1 CARTON (62756-460-64) / 10 TABLET in 1 BLISTER PACK
62756-460-836275604608330 TABLET in 1 BOTTLE (62756-460-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9fd1f18f-0b0f-4059-b603-19ecbf0ed63a

  • NADAC price for package 62756046083

    GET /v1/drugs/nadac/62756046083

Use it

Look up 62756-460 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-460 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-460. 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.