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NALTREXONE HYDROCHLORIDE

NDC 82804-199, NALTREXONE HYDROCHLORIDE, tablet, film coated, from Proficient Rx LP.

Product NDC
82804-199
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-199 \
  -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
82804-199-308280401993030 TABLET, FILM COATED in 1 BOTTLE (82804-199-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f3305f0b-fb9e-4009-b28f-47fe9b1b618b

Use it

Look up 82804-199 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-199 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-199. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.