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Famotidine

NDC 72657-112, Famotidine, tablet, film coated, from GLENMARK THERAPEUTICS INC., USA.

Product NDC
72657-112
Status
Listed
Labeler
GLENMARK THERAPEUTICS INC., USA
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215822
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72657-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72657-112-20726570112201 BOTTLE in 1 CARTON (72657-112-20) / 200 TABLET, FILM COATED in 1 BOTTLE
72657-112-90726570112901 BOTTLE in 1 CARTON (72657-112-90) / 90 TABLET, FILM COATED in 1 BOTTLE

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 72657-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72657-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72657-112. 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.