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Oxycodone and Acetaminophen

NDC 70010-669, Oxycodone and Acetaminophen, tablet, from Granules Pharmaceuticals Inc..

Product NDC
70010-669
Status
Listed
Labeler
Granules Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211708
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70010-669 \
  -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
70010-669-0170010066901100 TABLET in 1 BOTTLE (70010-669-01)
70010-669-0570010066905500 TABLET in 1 BOTTLE (70010-669-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cc966d57-7cdc-4de3-bbcf-718e2fce9cb7

  • NADAC price for package 70010066901

    GET /v1/drugs/nadac/70010066901

Use it

Look up 70010-669 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70010-669 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70010-669. 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.