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Famotidine

NDC 50090-7178, Famotidine, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-7178
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215767
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7178 \
  -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
50090-7178-05009071780030 TABLET, FILM COATED in 1 BOTTLE (50090-7178-0)
50090-7178-15009071780120 TABLET, FILM COATED in 1 BOTTLE (50090-7178-1)
50090-7178-25009071780260 TABLET, FILM COATED in 1 BOTTLE (50090-7178-2)
50090-7178-35009071780390 TABLET, FILM COATED in 1 BOTTLE (50090-7178-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0abfc8e6-7fdf-4828-89f4-2202002f8489

Use it

Look up 50090-7178 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7178 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7178. 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.