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FAMOTIDINE

NDC 68382-444, famotidine, powder, for suspension, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-444
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091020
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-444 \
  -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
68382-444-056838204440550 mL in 1 BOTTLE, PLASTIC (68382-444-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a8010e10-68fd-455f-968f-d62a1c3e0ffd

  • NADAC price for package 68382044405

    GET /v1/drugs/nadac/68382044405

Use it

Look up 68382-444 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-444 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-444. 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.