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Oxycodone Hydrochloride

NDC 72162-1336, Oxycodone Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
72162-1336
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091490
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1336 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE15 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1336-172162133601100 TABLET in 1 BOTTLE, PLASTIC (72162-1336-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0e4dd113-87ab-4a5d-846a-446db3cfd469

Use it

Look up 72162-1336 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1336 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1336. 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.