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Famotidine

NDC 48433-150, Famotidine, tablet, film coated, from Safecor Health, LLC.

Product NDC
48433-150
Status
Listed
Labeler
Safecor Health, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216441
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48433-150 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
48433-150-2048433015020100 BLISTER PACK in 1 CARTON (48433-150-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-150-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b5cb132-d28f-4fbe-91f5-dc04f9a551d1

Use it

Look up 48433-150 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48433-150 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48433-150. 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.