United States · FDA National Drug Code directory
Mannitol
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
- 0264-7578_33171b62-3532-4eb1-b273-714d07b0e3f8
- Product NDC
- 0264-7578
- Form
- INJECTION, SOLUTION
- Composition / generic term
- MANNITOL
- Labeler
- B. Braun Medical Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19930726
- Source listing expiry
- 20261231
Source-listed ingredients
- MANNITOL — 20 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 CONTAINER in 1 CASE (0264-7578-10) / 500 mL in 1 CONTAINER · 0264-7578-10
- 24 CONTAINER in 1 CASE (0264-7578-20) / 250 mL in 1 CONTAINER · 0264-7578-20
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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