Levetiracetam

Product NDC
70518-3582
11-digit product format
705183582
Labeler code
70518
Product ID
70518-3582_f0d1e9ab-eb7c-88f3-e053-2a95a90ab106
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
SOLUTION
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA079063
Marketing category
ANDA
Marketing start
2022-12-02
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 formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70518-3582-07051835820010 CUP, UNIT-DOSE in 1 BOX (70518-3582-0) > 12.5 mL in 1 CUP, UNIT-DOSE (70518-3582-2) 2022-12-020000-00-00NoNoCurrent
70518-3582-47051835820410 CUP, UNIT-DOSE in 1 BOX (70518-3582-4) > 15 mL in 1 CUP, UNIT-DOSE (70518-3582-5) 2022-12-070000-00-00NoNoCurrent
70518-3582-67051835820610 CUP, UNIT-DOSE in 1 BOX (70518-3582-6) > 20 mL in 1 CUP, UNIT-DOSE (70518-3582-3) 2022-12-080000-00-00NoNoCurrent
70518-3582-77051835820710 CUP, UNIT-DOSE in 1 BOX (70518-3582-7) > 7.5 mL in 1 CUP, UNIT-DOSE (70518-3582-8) 2022-12-080000-00-00NoNoCurrent
70518-3582-97051835820910 CUP, UNIT-DOSE in 1 BOX (70518-3582-9) > 10 mL in 1 CUP, UNIT-DOSE (70518-3582-1) 2022-12-020000-00-00NoNoCurrent