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famotidine

NDC 68475-400, famotidine, powder, for suspension, from Navinta LLC.

Product NDC
68475-400
Status
Listed
Labeler
Navinta LLC
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/68475-400 \
  -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
68475-400-016847504000150 mL in 1 BOTTLE, PLASTIC (68475-400-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f34a3be-7554-4040-b808-5ba8bf064abc

Use it

Look up 68475-400 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68475-400 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68475-400. 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.