Levetiracetam

Product NDC
70518-3192
11-digit product format
705183192
Labeler code
70518
Product ID
70518-3192_ccfe1fdb-4695-00a0-e053-2995a90a4749
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
SOLUTION
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA203052
Marketing category
ANDA
Marketing start
2021-08-12
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
70518-3192-07051831920010 CUP, UNIT-DOSE in 1 BOX (70518-3192-0) > 5 mL in 1 CUP, UNIT-DOSE (70518-3192-1) 2021-08-120000-00-00NoNoCurrent
70518-3192-2705183192027.5 mL in 1 CUP, UNIT-DOSE (70518-3192-2) 7.5 ml2021-08-120000-00-00NoNoCurrent
70518-3192-37051831920310 mL in 1 CUP, UNIT-DOSE (70518-3192-3) 10 ml2021-08-120000-00-00NoNoCurrent
70518-3192-47051831920412.5 mL in 1 CUP, UNIT-DOSE (70518-3192-4) 12.5 ml2021-08-120000-00-00NoNoCurrent
70518-3192-57051831920520 mL in 1 CUP, UNIT-DOSE (70518-3192-5) 20 ml2021-09-010000-00-00NoNoCurrent
70518-3192-67051831920615 mL in 1 CUP, UNIT-DOSE (70518-3192-6) 15 ml2021-09-270000-00-00NoNoCurrent