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Tylenol Extra Strength

NDC 50580-937, Acetaminophen, tablet, film coated, from Kenvue Brands LLC.

Product NDC
50580-937
Status
Listed
Labeler
Kenvue Brands LLC
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/50580-937 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN500 mg/1
Package NDCNDC-11Package
50580-937-015058009370112 VIAL in 1 PACKAGE (50580-937-01) / 10 TABLET, FILM COATED in 1 VIAL
50580-937-025058009370212 VIAL in 1 PACKAGE (50580-937-02) / 10 TABLET, FILM COATED in 1 VIAL
50580-937-06505800937061 BOTTLE in 1 CARTON (50580-937-06) / 24 TABLET, FILM COATED in 1 BOTTLE
50580-937-07505800937071 BOTTLE in 1 CARTON (50580-937-07) / 100 TABLET, FILM COATED in 1 BOTTLE
50580-937-10505800937101 BOTTLE in 1 CARTON (50580-937-10) / 50 TABLET, FILM COATED in 1 BOTTLE
50580-937-15505800937151 BOTTLE in 1 CARTON (50580-937-15) / 225 TABLET, FILM COATED in 1 BOTTLE
50580-937-1950580093719325 TABLET, FILM COATED in 1 BOTTLE (50580-937-19)
50580-937-23505800937233 POUCH in 1 CARTON (50580-937-23) / 2 TABLET, FILM COATED in 1 POUCH
50580-937-25505800937252500 POUCH in 1 CASE (50580-937-25) / 2 TABLET, FILM COATED in 1 POUCH
50580-937-3750580093737320 TABLET, FILM COATED in 1 BOTTLE (50580-937-37)
50580-937-505058009375050 POUCH in 1 CARTON (50580-937-50) / 2 TABLET, FILM COATED in 1 POUCH
50580-937-515058009375150 POUCH in 1 CARTON (50580-937-51) / 2 TABLET, FILM COATED in 1 POUCH
50580-937-66505800937662 BOTTLE in 1 CARTON (50580-937-66) / 100 TABLET, FILM COATED 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 50580-937 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50580-937 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50580-937. 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.