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Zantac 360

NDC 85237-1926, Famotidine, tablet, film coated, from Select Consumer Group LLC.

Product NDC
85237-1926
Status
Listed
Labeler
Select Consumer Group LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206531
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85237-1926 \
  -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
85237-1926-1852371926011 BLISTER PACK in 1 CONTAINER (85237-1926-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0)
85237-1926-2852371926022 BLISTER PACK in 1 CONTAINER (85237-1926-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0)

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 85237-1926 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85237-1926 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85237-1926. 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.