United States · FDA National Drug Code directory
Famotidine
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
- 55111-396_e818465f-a1ca-0e6a-f18c-cf2cb2a2cc82
- Product NDC
- 55111-396
- Form
- TABLET
- Composition / generic term
- Famotidine
- Labeler
- Dr.Reddys Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060930
- Source listing expiry
- 20261231
Source-listed ingredients
- FAMOTIDINE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (55111-396-01) / 100 TABLET in 1 BOTTLE · 55111-396-01
- 1 BLISTER PACK in 1 CARTON (55111-396-08) / 8 TABLET in 1 BLISTER PACK · 55111-396-08
- 1 BOTTLE in 1 CARTON (55111-396-13) / 130 TABLET in 1 BOTTLE · 55111-396-13
- 5 BLISTER PACK in 1 CARTON (55111-396-16) / 5 TABLET in 1 BLISTER PACK · 55111-396-16
- 1 BOTTLE in 1 CARTON (55111-396-32) / 170 TABLET in 1 BOTTLE · 55111-396-32
- 1 BOTTLE in 1 CARTON (55111-396-35) / 25 TABLET in 1 BOTTLE · 55111-396-35
- 2 BOTTLE in 1 CARTON (55111-396-44) / 100 TABLET in 1 BOTTLE · 55111-396-44
- 1 BOTTLE in 1 CARTON (55111-396-50) / 50 TABLET in 1 BOTTLE · 55111-396-50
- 1 BOTTLE in 1 CARTON (55111-396-65) / 65 TABLET in 1 BOTTLE · 55111-396-65
- 1 BOTTLE in 1 CARTON (55111-396-90) / 90 TABLET in 1 BOTTLE · 55111-396-90
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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