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Pain Relief

NDC 41250-802, Acetaminophen, tablet, film coated, extended release, from Meijer Distribution Inc.

Product NDC
41250-802
Status
Listed
Labeler
Meijer Distribution Inc
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075077
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/41250-802 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
41250-802-62412500802621 BOTTLE in 1 CARTON (41250-802-62) / 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
41250-802-78412500802781 BOTTLE in 1 CARTON (41250-802-78) / 100 TABLET, FILM COATED, 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 41250-802 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/41250-802 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 41250-802. 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.