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Famotidine

NDC 70771-1702, Famotidine, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1702
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/70771-1702 \
  -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
70771-1702-0707711702001000 TABLET, FILM COATED in 1 BOTTLE (70771-1702-0)
70771-1702-170771170201100 TABLET, FILM COATED in 1 BOTTLE (70771-1702-1)
70771-1702-37077117020330 TABLET, FILM COATED in 1 BOTTLE (70771-1702-3)
70771-1702-47077117020410 BLISTER PACK in 1 CARTON (70771-1702-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1702-2)
70771-1702-570771170205500 TABLET, FILM COATED in 1 BOTTLE (70771-1702-5)

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 70771-1702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1702. 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.