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Buprenorphine

NDC 0054-0176, Buprenorphine, tablet, from Hikma Pharmaceuticals USA Inc..

Product NDC
0054-0176
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078633
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0176 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0054-0176-130005401761330 TABLET in 1 BOTTLE (0054-0176-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1bf8b35a-b769-465c-a2f8-099868dfcd2f

  • NADAC price for package 00054017613

    GET /v1/drugs/nadac/00054017613

Use it

Look up 0054-0176 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0176 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0054-0176. 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.