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Famotidine

NDC 70771-1703, Famotidine, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1703
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1703 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1703-0707711703001000 TABLET, FILM COATED in 1 BOTTLE (70771-1703-0)
70771-1703-170771170301100 TABLET, FILM COATED in 1 BOTTLE (70771-1703-1)
70771-1703-37077117030330 TABLET, FILM COATED in 1 BOTTLE (70771-1703-3)
70771-1703-47077117030410 BLISTER PACK in 1 CARTON (70771-1703-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1703-2)
70771-1703-570771170305500 TABLET, FILM COATED in 1 BOTTLE (70771-1703-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c17f9e3-9827-4bf9-85ca-72e08a8518ca

Use it

Look up 70771-1703 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1703 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1703. 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.