United States · FDA National Drug Code directory

Original strength heartburn prevention

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
41226-719_1cb86ee4-41c1-1196-e063-6394a90a9199
Product NDC
41226-719
Form
TABLET
Composition / generic term
Famotidine
Labeler
KROGER COMPANY
Marketing category
ANDA
Marketing start / end (source format)
20230505
Source listing expiry
20261231

Source-listed ingredients

  • FAMOTIDINE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BLISTER PACK in 1 CARTON (41226-719-06) / 10 TABLET in 1 BLISTER PACK · 41226-719-06
  • 1 BOTTLE in 1 CARTON (41226-719-09) / 90 TABLET in 1 BOTTLE · 41226-719-09

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →