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IBUPROFEN

NDC 11822-7891, IBUPROFEN, tablet, coated, from RITE AID CORPORATION.

Product NDC
11822-7891
Status
Listed
Labeler
RITE AID CORPORATION
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA091239
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11822-7891 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
11822-7891-21182278910250 TABLET, COATED in 1 BOTTLE (11822-7891-2)
11822-7891-511822789105100 TABLET, COATED in 1 BOTTLE (11822-7891-5)
11822-7891-911822789109500 TABLET, COATED in 1 BOTTLE (11822-7891-9)

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 11822-7891 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11822-7891 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11822-7891. 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.