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Famotidine

NDC 0832-6045, Famotidine, powder, for suspension, from Upsher-Smith Laboratories, LLC.

Product NDC
0832-6045
Status
Listed
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217655
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0832-6045 \
  -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
0832-6045-1000832604510100 mL in 1 BOTTLE (0832-6045-10)
0832-6045-1500832604515150 mL in 1 BOTTLE (0832-6045-15)
0832-6045-500083260455050 mL in 1 BOTTLE (0832-6045-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d528fadf-316f-4fea-9bec-070c01f80d64

  • NADAC price for package 00832604510

    GET /v1/drugs/nadac/00832604510

  • NADAC price for package 00832604550

    GET /v1/drugs/nadac/00832604550

Use it

Look up 0832-6045 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0832-6045 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0832-6045. 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.