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buprenorphine hydrochloride

NDC 72888-510, buprenorphine hydrochloride, tablet, from Advagen Pharma Ltd.

Product NDC
72888-510
Status
Listed
Labeler
Advagen Pharma Ltd
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090279
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72888-510 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE12 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72888-510-017288805100130 TABLET in 1 BOTTLE (72888-510-01)
72888-510-027288805100290 TABLET in 1 BOTTLE (72888-510-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/699638dd-3a53-445f-a545-d0e6eabfe1c9

Use it

Look up 72888-510 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72888-510 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72888-510. 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.