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Famotidine

NDC 46708-294, Famotidine, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-294
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-294 \
  -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
46708-294-1046708029410100 TABLET in 1 CARTON (46708-294-10)
46708-294-304670802943030 TABLET in 1 BOTTLE (46708-294-30)
46708-294-3146708029431100 TABLET in 1 BOTTLE (46708-294-31)
46708-294-7146708029471500 TABLET in 1 BOTTLE (46708-294-71)
46708-294-91467080294911000 TABLET in 1 BOTTLE (46708-294-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7c0f3fa5-0a44-4a98-bc43-8bff8e95c462

Use it

Look up 46708-294 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-294 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-294. 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.