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Curist Acid Relief

NDC 72559-032, Famotidine 20 mg, tablet, from Little Pharma, Inc..

Product NDC
72559-032
Status
Listed
Labeler
Little Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215822
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72559-032 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72559-032-2272559003222200 TABLET in 1 BOTTLE (72559-032-22)
72559-032-2372559003223300 TABLET in 1 BOTTLE (72559-032-23)
72559-032-6372559003263500 TABLET in 1 BOTTLE (72559-032-63)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 72559-032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72559-032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72559-032. 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.