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buprenorphine hydrochloride

NDC 50090-7559, buprenorphine hydrochloride, tablet, from A-S Medication Solutions.

Product NDC
50090-7559
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090622
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7559 \
  -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
50090-7559-05009075590030 TABLET in 1 BOTTLE (50090-7559-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c1398d85-d4bb-4426-8ecf-a50400910d81

Use it

Look up 50090-7559 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7559 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7559. 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.