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Acetaminophen

NDC 69848-015, Acetaminophen, tablet, film coated, extended release, from Granules USA, Inc..

Product NDC
69848-015
Status
Listed
Labeler
Granules USA, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211544
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69848-015 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
69848-015-1069848001510100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-10)
69848-015-246984800152424 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-24)

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 69848-015 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69848-015 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69848-015. 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.