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Acetaminophen Extended-Release Tablets, 650 mg

NDC 25000-108, Acetaminophen, tablet, extended release, from MARKSANS PHARMA LIMITED.

Product NDC
25000-108
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215486
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
25000-108-02250000108021 BOTTLE in 1 CARTON (25000-108-02) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
25000-108-08250000108081 BOTTLE in 1 CARTON (25000-108-08) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 25000-108 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-108. 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.