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Oxycodone Hydrochloride and Acetaminophen

NDC 64850-622, Oxycodone Hydrochloride and Acetaminophen, tablet, from Elite Laboratories, Inc..

Product NDC
64850-622
Status
Listed
Labeler
Elite Laboratories, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209385
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64850-622 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE7.5 mg/1
  • ACETAMINOPHEN325 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
64850-622-0164850062201100 TABLET in 1 BOTTLE (64850-622-01)
64850-622-0564850062205500 TABLET in 1 BOTTLE (64850-622-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/27fa8190-d334-4bb9-b277-d1f44db433e3

  • NADAC price for package 64850062201

    GET /v1/drugs/nadac/64850062201

Use it

Look up 64850-622 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64850-622 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64850-622. 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.