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Famotidine

NDC 46708-293, Famotidine, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-293
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/46708-293 \
  -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
46708-293-1046708029310100 TABLET in 1 CARTON (46708-293-10)
46708-293-304670802933030 TABLET in 1 BOTTLE (46708-293-30)
46708-293-3146708029331100 TABLET in 1 BOTTLE (46708-293-31)
46708-293-7146708029371500 TABLET in 1 BOTTLE (46708-293-71)
46708-293-91467080293911000 TABLET in 1 BOTTLE (46708-293-91)

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 46708-293 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-293 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-293. 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.