United States · FDA National Drug Code directory
Galantamine Hydrobromide
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
- 0054-0137_b2bf3efc-7521-4ff7-b77c-6e312e34b3c4
- Product NDC
- 0054-0137
- Form
- SOLUTION
- Composition / generic term
- Galantamine Hydrobromide
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090814
- Source listing expiry
- 20261231
Source-listed ingredients
- GALANTAMINE HYDROBROMIDE — 4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 100 mL in 1 BOTTLE (0054-0137-49) · 0054-0137-49
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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