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Buprenorphine

NDC 70518-1557, Buprenorphine, tablet, from REMEDYREPACK INC..

Product NDC
70518-1557
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090819
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1557 \
  -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
70518-1557-17051815570150 POUCH in 1 BOX (70518-1557-1) / 1 TABLET in 1 POUCH (70518-1557-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aa86a438-1ebf-4c08-bf27-38f1e81efb3a

Use it

Look up 70518-1557 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1557 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1557. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.