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Oxycodone Hydrochloride

NDC 68071-2899, Oxycodone Hydrochloride, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2899
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-2899 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-2899-4680712899044 TABLET in 1 BOTTLE, PLASTIC (68071-2899-4)
68071-2899-6680712899066 TABLET in 1 BOTTLE, PLASTIC (68071-2899-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ef58f422-682e-6896-e053-2a95a90a1f2d

Use it

Look up 68071-2899 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2899 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2899. 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.