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IBUPROFEN

NDC 58602-913, IBUPROFEN, tablet, from Aurohealth LLC.

Product NDC
58602-913
Status
Listed
Labeler
Aurohealth LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA208865
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58602-913 \
  -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
58602-913-17586020913171000 TABLET in 1 BOTTLE (58602-913-17)
58602-913-4058602091340500 TABLET in 1 BOTTLE (58602-913-40)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 58602-913 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58602-913 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58602-913. 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.