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Famotidine

NDC 46122-735, Famotidine, tablet, film coated, from Amerisource Bergen.

Product NDC
46122-735
Status
Listed
Labeler
Amerisource Bergen
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206531
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46122-735 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
46122-735-65461220735651 BOTTLE in 1 CARTON (46122-735-65) / 30 TABLET, FILM COATED in 1 BOTTLE
46122-735-75461220735751 BOTTLE in 1 CARTON (46122-735-75) / 90 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 46122073565

    GET /v1/drugs/nadac/46122073565
  • NADAC price for package 46122073575

    GET /v1/drugs/nadac/46122073575

Use it

Look up 46122-735 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46122-735 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46122-735. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.