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Ibuprofen and famotidine

NDC 59651-908, Ibuprofen and famotidine, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
59651-908
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219538
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-908 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN800 mg/1
  • FAMOTIDINE26.6 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
59651-908-905965109089090 TABLET, FILM COATED in 1 BOTTLE (59651-908-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/21688404-41fb-487e-8ba0-aea4431a42fa

Use it

Look up 59651-908 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-908 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.