United States · FDA National Drug Code directory

acid reducer complete

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
21130-786_323b0cda-6d60-4877-97e6-4f60552642c0
Product NDC
21130-786
Form
TABLET, CHEWABLE
Composition / generic term
Famotidine, Calcium Carbonate, Magnesium Hydroxide
Labeler
Safeway
Marketing category
ANDA
Marketing start / end (source format)
20250922
Source listing expiry
20261231

Source-listed ingredients

  • FAMOTIDINE — 10 mg/1
  • CALCIUM CARBONATE — 800 mg/1
  • MAGNESIUM HYDROXIDE — 165 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 TABLET, CHEWABLE in 1 BOTTLE (21130-786-63) · 21130-786-63
  • 50 TABLET, CHEWABLE in 1 BOTTLE (21130-786-71) · 21130-786-71

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 →