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
- 0121-0727_d56a22ea-5dab-e98a-e053-2a95a90a34c4
- Product NDC
- 0121-0727
- Form
- SYRUP
- Composition / generic term
- RANITIDINE
- Labeler
- Pharmaceutical Associates, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101101
- Source listing expiry
- 20261231
Source-listed ingredients
- RANITIDINE — 15 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (0121-0727-16) · 0121-0727-16
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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