United States · FDA National Drug Code directory
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
- 56062-088_b3862f03-3efe-4e65-a637-46441e9ab01f
- Product NDC
- 56062-088
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- Publix Super Markets Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260306
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25 BLISTER PACK in 1 CARTON (56062-088-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 56062-088-02
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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