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Zantac 360

NDC 66715-9758, Famotidine tablet, film-coated, tablet, film coated, from Lil' Drug Store Products, Inc.

Product NDC
66715-9758
Status
Listed
Labeler
Lil' Drug Store Products, Inc
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/66715-9758 \
  -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
66715-9758-2667159758021 BLISTER PACK in 1 CARTON (66715-9758-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK
66715-9758-5667159758051 BLISTER PACK in 1 CARTON (66715-9758-5) / 5 TABLET, FILM COATED in 1 BLISTER PACK

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 66715-9758 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66715-9758 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66715-9758. 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.