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Prolate

NDC 72245-682, oxycodone and acetaminophen, tablet, from Forte Bio-Pharma LLC.

Product NDC
72245-682
Status
Listed
Labeler
Forte Bio-Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040608
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72245-682 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE7.5 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72245-682-037224506820330 TABLET in 1 BOTTLE, PLASTIC (72245-682-03)
72245-682-1072245068210100 TABLET in 1 BOTTLE, PLASTIC (72245-682-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cbbfa94-37b9-9652-e053-2995a90a736b

Use it

Look up 72245-682 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72245-682 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72245-682. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.