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NALTREXONE HYDROCHLORIDE

NDC 68084-291, naltrexone hydrochloride, tablet, film coated, from American Health Packaging.

Product NDC
68084-291
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076264
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68084-291 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALTREXONE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
68084-291-216808402912130 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/81e25c6a-81b6-4cfb-91bf-be20c3ae546b

  • NADAC price for package 68084029121

    GET /v1/drugs/nadac/68084029121

Use it

Look up 68084-291 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68084-291 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68084-291. 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.