United States · FDA National Drug Code directory

Osmitrol

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
0338-0353_3911fd42-2b73-4509-9c4c-92ceba4e6d34
Product NDC
0338-0353
Form
INJECTION, SOLUTION
Composition / generic term
Mannitol
Labeler
Baxter Healthcare Company
Marketing category
NDA
Marketing start / end (source format)
19640608
Source listing expiry
20261231

Source-listed ingredients

  • MANNITOL — 10 g/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 mL in 1 BAG (0338-0353-03) · 0338-0353-03

Source and coverage

Open FDA National Drug Code directory

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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