Mannitol

Product NDC
0264-2303
11-digit product format
002642303
Labeler code
0264
Product ID
0264-2303_6d040194-f4be-4fcf-b571-91cb722e0ceb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mannitol
Dosage form
IRRIGANT
Route
IRRIGATION
Labeler
B. Braun Medical Inc.
Application
NDA016772
Marketing category
NDA
Marketing start
1978-02-10
Marketing end
0000-00-00
Substance
MANNITOL
Active strength
5 g/100mL
Pharmacologic classes
Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0264-2303-50ML - Milliliter0264-23037b8a1765-d808-46e2-883f-705407c50cb112012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0264-2303-50002642303508 CONTAINER in 1 CASE (0264-2303-50) > 2000 mL in 1 CONTAINER8 container1978-02-100000-00-00NoNoCurrent
0264-2303-70002642303704 CONTAINER in 1 CASE (0264-2303-70) > 4000 mL in 1 CONTAINER4 container1978-02-100000-00-00NoNoCurrent