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Acetaminophen

NDC 69842-322, Acetaminophen, tablet, film coated, extended release, from CVS PHARMACY INC.

Product NDC
69842-322
Status
Listed
Labeler
CVS PHARMACY INC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211544
DEA schedule
None
Request
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  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
69842-322-1069842032210100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69842-322-10)
69842-322-246984203222424 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69842-322-24)

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 69842-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69842-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69842-322. 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.