LEVETIRACETAM

Product NDC
70518-2328
11-digit product format
705182328
Labeler code
70518
Product ID
70518-2328_db60df21-bc16-1c9e-e053-2995a90aae78
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LEVETIRACETAM
Dosage form
SOLUTION
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA079120
Marketing category
ANDA
Marketing start
2019-10-02
Marketing end
0000-00-00
Substance
LEVETIRACETAM
Active strength
100 mg/mL
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-2328-07051823280010 CUP, UNIT-DOSE in 1 BOX (70518-2328-0) > 20 mL in 1 CUP, UNIT-DOSE (70518-2328-1) 2019-10-020000-00-00NoNoCurrent
70518-2328-27051823280212.5 mL in 1 CUP, UNIT-DOSE (70518-2328-2) 12.5 ml2020-07-060000-00-00NoNoCurrent
70518-2328-37051823280315 mL in 1 CUP, UNIT-DOSE (70518-2328-3) 15 ml2020-07-300000-00-00NoNoCurrent
70518-2328-47051823280410 mL in 1 CUP, UNIT-DOSE (70518-2328-4) 10 ml2020-07-300000-00-00NoNoCurrent
70518-2328-5705182328057.5 mL in 1 CUP, UNIT-DOSE (70518-2328-5) 7.5 ml2020-07-300000-00-00NoNoCurrent
70518-2328-6705182328065 mL in 1 CUP, UNIT-DOSE (70518-2328-6) 5 ml2020-07-300000-00-00NoNoCurrent