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Buprenorphine HCl

NDC 70518-2014, Buprenorphine HCl, tablet, from REMEDYREPACK INC..

Product NDC
70518-2014
Status
Listed
Labeler
REMEDYREPACK 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/70518-2014 \
  -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
70518-2014-07051820140030 TABLET in 1 BLISTER PACK (70518-2014-0)
70518-2014-270518201402100 POUCH in 1 BOX (70518-2014-2) / 1 TABLET in 1 POUCH (70518-2014-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/69a647c0-bc09-4ee2-aeb3-ef286caf25e5

Use it

Look up 70518-2014 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2014 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2014. 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.