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Oxycodone Hydrochloride

NDC 72162-1335, Oxycodone Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
72162-1335
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/72162-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1335-272162133502120 TABLET in 1 BOTTLE (72162-1335-2)
72162-1335-37216213350330 TABLET in 1 BOTTLE (72162-1335-3)
72162-1335-67216213350660 TABLET in 1 BOTTLE (72162-1335-6)
72162-1335-97216213350990 TABLET in 1 BOTTLE (72162-1335-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a1e539ba-2cb5-4815-8c58-37abfd978fa5

Use it

Look up 72162-1335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1335. 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.