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Famotidine

NDC 69842-063, Famotidine, tablet, film coated, from CVS Pharmacy, Inc..

Product NDC
69842-063
Status
Listed
Labeler
CVS Pharmacy, 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/69842-063 \
  -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
69842-063-19698420063191 BOTTLE in 1 CARTON (69842-063-19) / 90 TABLET, FILM COATED in 1 BOTTLE
69842-063-79698420063792 BOTTLE in 1 CARTON (69842-063-79) / 90 TABLET, FILM COATED in 1 BOTTLE
69842-063-84698420063841 BOTTLE in 1 CARTON (69842-063-84) / 30 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 69842-063 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69842-063 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69842-063. 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.