United States · FDA National Drug Code directory
Ranitidine
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
- 55111-131_210e3c0b-be93-aa50-550d-e383e7d5f19e
- Product NDC
- 55111-131
- Form
- TABLET
- Composition / generic term
- Ranitidine
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20000301
- Source listing expiry
- 20261231
Source-listed ingredients
- RANITIDINE HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (55111-131-04) / 120 TABLET in 1 BOTTLE · 55111-131-04
- 2 BLISTER PACK in 1 CARTON (55111-131-14) / 10 TABLET in 1 BLISTER PACK · 55111-131-14
- 1 BOTTLE in 1 CARTON (55111-131-30) / 30 TABLET in 1 BOTTLE · 55111-131-30
- 1 BOTTLE in 1 CARTON (55111-131-37) / 160 TABLET in 1 BOTTLE · 55111-131-37
- 1 BOTTLE in 1 CARTON (55111-131-45) / 45 TABLET in 1 BOTTLE · 55111-131-45
- 1 BOTTLE in 1 CARTON (55111-131-60) / 60 TABLET in 1 BOTTLE · 55111-131-60
- 1 BLISTER PACK in 1 CARTON (55111-131-79) / 10 TABLET in 1 BLISTER PACK · 55111-131-79
- 1 BOTTLE in 1 CARTON (55111-131-80) / 80 TABLET in 1 BOTTLE · 55111-131-80
- 3 BLISTER PACK in 1 CARTON (55111-131-81) / 10 TABLET in 1 BLISTER PACK · 55111-131-81
- 1 BOTTLE in 1 CARTON (55111-131-90) / 90 TABLET in 1 BOTTLE · 55111-131-90
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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