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Famotidine

NDC 0527-5190, Famotidine, powder, for suspension, from Lannett Company, Inc..

Product NDC
0527-5190
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217982
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0527-5190 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
0527-5190-800052751908055 mL in 1 BOTTLE (0527-5190-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7e0da8be-b001-400e-99d1-37f335b1d7b3

Use it

Look up 0527-5190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0527-5190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0527-5190. 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.