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famotidine

NDC 62135-808, famotidine, tablet, film coated, from Chartwell RX, LLC.

Product NDC
62135-808
Status
Listed
Labeler
Chartwell RX, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075786
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62135-808 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62135-808-906213508089090 TABLET, FILM COATED in 1 BOTTLE (62135-808-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/70714491-1368-4824-98af-03fda52139a9
  • NADAC price for package 62135080890

    GET /v1/drugs/nadac/62135080890

Use it

Look up 62135-808 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62135-808 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62135-808. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.