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
- 66715-9758_274bc24b-823e-516d-e063-6394a90a2680
- Product NDC
- 66715-9758
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine tablet, film-coated
- Labeler
- Lil' Drug Store Products, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210920
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (66715-9758-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK · 66715-9758-2
- 1 BLISTER PACK in 1 CARTON (66715-9758-5) / 5 TABLET, FILM COATED in 1 BLISTER PACK · 66715-9758-5
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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