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Ibuprofen and Famotidine

NDC 70771-1924, Ibuprofen and Famotidine, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1924
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218684
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1924 \
  -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
70771-1924-97077119240990 TABLET in 1 BOTTLE (70771-1924-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/24204938-0989-42ad-8ad8-89979e62d700

Use it

Look up 70771-1924 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1924 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1924. 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.