United States · FDA National Drug Code directory
Curist Acid Relief
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
- 72559-032_56c07eb7-07fe-00c1-e063-6394a90aa202
- Product NDC
- 72559-032
- Form
- TABLET
- Composition / generic term
- Famotidine 20 mg
- Labeler
- Little Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240131
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 200 TABLET in 1 BOTTLE (72559-032-22) · 72559-032-22
- 300 TABLET in 1 BOTTLE (72559-032-23) · 72559-032-23
- 500 TABLET in 1 BOTTLE (72559-032-63) · 72559-032-63
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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