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8 hr Arthritis Pain Relief

NDC 55910-892, Acetaminophen, tablet, extended release, from DOLGENCORP, INC..

Product NDC
55910-892
Status
Listed
Labeler
DOLGENCORP, INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215486
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55910-892 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN650 mg/1
Package NDCNDC-11Package
55910-892-05559100892051 BOTTLE in 1 CARTON (55910-892-05) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE
55910-892-26559100892261 BOTTLE in 1 CARTON (55910-892-26) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE
55910-892-42559100892421 BOTTLE in 1 CARTON (55910-892-42) / 24 TABLET, EXTENDED RELEASE 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 55910-892 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55910-892 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55910-892. 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.