United States · FDA National Drug Code directory
Zantac 360
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
- 85237-1926_554485e1-6776-5eb3-e063-6394a90a7c6b
- Product NDC
- 85237-1926
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- Select Consumer Group LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210412
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CONTAINER (85237-1926-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0) · 85237-1926-1
- 2 BLISTER PACK in 1 CONTAINER (85237-1926-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK (85237-1926-0) · 85237-1926-2
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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