Levetiracetam

Product NDC
70518-1969
11-digit product format
705181969
Labeler code
70518
Product ID
70518-1969_c716d883-49f8-0833-e053-2995a90a3dfa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LEVETIRACETAM
Dosage form
SOLUTION
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA201157
Marketing category
ANDA
Marketing start
2019-11-03
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-1969-07051819690010 CUP, UNIT-DOSE in 1 BOX (70518-1969-0) > 20 mL in 1 CUP, UNIT-DOSE (70518-1969-1) 2019-11-030000-00-00NoNoCurrent
70518-1969-27051819690215 mL in 1 CUP, UNIT-DOSE (70518-1969-2) 15 ml2019-11-030000-00-00NoNoCurrent
70518-1969-37051819690312.5 mL in 1 CUP, UNIT-DOSE (70518-1969-3) 12.5 ml2019-11-030000-00-00NoNoCurrent
70518-1969-47051819690410 mL in 1 CUP, UNIT-DOSE (70518-1969-4) 10 ml2019-11-030000-00-00NoNoCurrent
70518-1969-5705181969057.5 mL in 1 CUP, UNIT-DOSE (70518-1969-5) 7.5 ml2019-11-030000-00-00NoNoCurrent
70518-1969-6705181969065 mL in 1 CUP, UNIT-DOSE (70518-1969-6) 5 ml2020-05-190000-00-00NoNoCurrent