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Famotidine

NDC 70518-4395, Famotidine, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4395
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217400
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4395 \
  -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
70518-4395-07051843950030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4395-0)
70518-4395-17051843950150 POUCH in 1 BOX (70518-4395-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4395-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8dbf43e0-856f-443b-b8a4-c69e006878ea

Use it

Look up 70518-4395 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4395 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4395. 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.