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PANADOL Extra Strength

NDC 0135-7011, acetaminophen, tablet, film coated, from Haleon US Holdings LLC.

Product NDC
0135-7011
Status
Listed
Labeler
Haleon US Holdings 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/0135-7011 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN500 mg/1
Package NDCNDC-11Package
0135-7011-01001357011012 TABLET, FILM COATED in 1 POUCH (0135-7011-01)
0135-7011-02001357011021 BOTTLE in 1 CARTON (0135-7011-02) / 24 TABLET, FILM COATED in 1 BOTTLE
0135-7011-03001357011031 BOTTLE in 1 CARTON (0135-7011-03) / 50 TABLET, FILM COATED in 1 BOTTLE
0135-7011-04001357011041 BOTTLE in 1 CARTON (0135-7011-04) / 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 0135-7011 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0135-7011 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0135-7011. 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.