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Uline Acetaminophen Extra Strength

NDC 69790-804, acetaminophen, tablet, film coated, from Uline.

Product NDC
69790-804
Status
Listed
Labeler
Uline
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M013
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69790-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN500 mg/1
Package NDCNDC-11Package
69790-804-336979008043350 PACKET in 1 BOX (69790-804-33) / 2 TABLET, FILM COATED in 1 PACKET

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 69790-804 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69790-804 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69790-804. 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.