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FAMOTIDINE

NDC 59651-701, FAMOTIDINE, powder, for suspension, from Aurobindo Pharma Limited.

Product NDC
59651-701
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219091
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
59651-701-505965107015050 mL in 1 BOTTLE (59651-701-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/18066b80-1ec6-4092-80d9-70adb0ecac85

  • NADAC price for package 59651070150

    GET /v1/drugs/nadac/59651070150

Use it

Look up 59651-701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-701. 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.