Levetiracetam

Product NDC
63629-5038
11-digit product format
636295038
Labeler code
63629
Product ID
63629-5038_0c5ad3e8-a196-457f-8ca8-063d33cf1261
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078154
Marketing category
ANDA
Marketing start
2009-01-01
Marketing end
0000-00-00
Substance
LEVETIRACETAM
Active strength
750 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-5038-1EA - Each63629-50381374eb50-e887-42a0-8800-a126ac4c706712015-10-02
63629-5038-2EA - Each63629-5038b4bf6189-075a-4791-ab18-e907017e2b8212015-10-02