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Buprenorphine hydrochloride

NDC 68083-696, Buprenorphine hydrochloride, injection, from Gland Pharma Limited.

Product NDC
68083-696
Status
Listed
Labeler
Gland Pharma Limited
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA221145
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68083-696 \
  -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
68083-696-05680830696055 VIAL in 1 CARTON (68083-696-05) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/69ec3405-78ee-4cb4-9180-9bea937a8dcd

Use it

Look up 68083-696 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68083-696 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.