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Acetaminophen and Ibuprofen

NDC 50844-598, Acetaminophen, Ibuprofen, tablet, film coated, from L.N.K. International, Inc..

Product NDC
50844-598
Status
Listed
Labeler
L.N.K. International, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA220126
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50844-598 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN250 mg/1
  • IBUPROFEN125 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
50844-598-1450844059814500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-598-14)
50844-598-19508440598191 BOTTLE, PLASTIC in 1 CARTON (50844-598-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

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 50844-598 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50844-598 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50844-598. 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.