United States · FDA National Drug Code directory

basic care acid reducer

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
72288-194_c2571299-d298-49de-84b3-be58dd9451ec
Product NDC
72288-194
Form
TABLET, FILM COATED
Composition / generic term
Famotidine
Labeler
Amazon.com Services LLC
Marketing category
ANDA
Marketing start / end (source format)
20201006
Source listing expiry
20261231

Source-listed ingredients

  • FAMOTIDINE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 BOTTLE in 1 CARTON (72288-194-00) / 200 TABLET, FILM COATED in 1 BOTTLE · 72288-194-00
  • 25 BLISTER PACK in 1 CARTON (72288-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 72288-194-02
  • 1 BOTTLE in 1 CARTON (72288-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 72288-194-71
  • 1 BOTTLE in 1 CARTON (72288-194-82) / 200 TABLET, FILM COATED in 1 BOTTLE · 72288-194-82

Source and coverage

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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.

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