LEVETIRACETAM

Product NDC
0121-4802
11-digit product format
001214802
Labeler code
0121
Product ID
0121-4802_6896783a-f114-4488-8538-2cd46eb21460
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LEVETIRACETAM
Dosage form
SOLUTION
Route
ORAL
Labeler
Pharmaceutical Associates, Inc.
Application
ANDA090028
Marketing category
ANDA
Marketing start
2009-02-11
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0121-4802-05ML - Milliliter0121-480215a5b3ed-825b-45b0-b13c-b4c8238f454112012-07-24