United States · FDA National Drug Code directory
Maximum Strength 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
- 11673-697_18567eaf-6b97-8c6f-e063-6294a90a986d
- Product NDC
- 11673-697
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- TARGET CORPORATION
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240515
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (11673-697-01) / 50 TABLET in 1 BOTTLE · 11673-697-01
- 1 BOTTLE in 1 CARTON (11673-697-05) / 50 TABLET in 1 BOTTLE · 11673-697-05
- 1 BOTTLE in 1 CARTON (11673-697-20) / 200 TABLET in 1 BOTTLE · 11673-697-20
- 5 BLISTER PACK in 1 CARTON (11673-697-52) / 5 TABLET in 1 BLISTER PACK · 11673-697-52
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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