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FAMOTIDINE

NDC 72603-564, FAMOTIDINE, powder, for suspension, from NorthStar Rx LLC.

Product NDC
72603-564
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219091
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-564 \
  -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
72603-564-017260305640150 mL in 1 BOTTLE (72603-564-01)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4af90b5d-f47a-4436-8e24-4cb7e5b758b3

Use it

Look up 72603-564 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-564 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-564. 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.