Isolyte S in Dextrose

Product NDC
0264-7704
11-digit product format
002647704
Labeler code
0264
Product ID
0264-7704_cb81fe4a-10a7-4e24-aa4f-b4315fcfe39b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrous Dextrose, Sodium Chloride, Sodium Gluconate, Sodium Acetate Trihydrate, Potassium Chloride a
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
B. Braun Medical Inc.
Application
ANDA019843
Marketing category
ANDA
Marketing start
1993-08-09
Marketing end
0000-00-00
Substance
DEXTROSE; SODIU
Active strength
5 g/100mL; g/100m
Pharmacologic classes
Osmotic Laxativ
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0264-7704-00ML - Milliliter0264-7704100ea96e-9504-4ce2-9948-af1b647f439812012-07-24