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Buprenorphine Hydrochloride

NDC 70069-027, Buprenorphine Hydrochloride, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-027
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219302
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE.324 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70069-027-05700690027055 VIAL in 1 CARTON (70069-027-05) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/74e40c51-853b-4e7f-b3cb-a27af29e1cbf

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-027

Use it

Look up 70069-027 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-027. 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.