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Buprenorphine and Naloxone

NDC 43598-582, Buprenorphine and Naloxone, film, soluble, from Dr.Reddys Laboratories Inc.

Product NDC
43598-582
Status
Listed
Labeler
Dr.Reddys Laboratories Inc
Dosage form
FILM, SOLUBLE
Route
BUCCAL, SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205299
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-582 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE8 mg/1
  • NALOXONE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43598-582-304359805823030 POUCH in 1 CARTON (43598-582-30) / 1 FILM, SOLUBLE in 1 POUCH (43598-582-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/718756d7-0131-b173-6c45-5ee039b311b0

  • NADAC price for package 43598058230

    GET /v1/drugs/nadac/43598058230

Use it

Look up 43598-582 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-582 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-582. 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.