ROWEEPRA

Product NDC
69102-102
11-digit product format
691020102
Labeler code
69102
Product ID
69102-102_e8c79c4a-d4e1-0a76-467f-e5c6283750b1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
levetiracetam
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
OWP Pharmaceuticals, Inc.
Application
ANDA090906
Marketing category
ANDA
Marketing start
2017-03-30
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
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69102-102-01EA - Each69102-102209f7f93-9994-46e6-b61e-7934ca9b37be12017-05-04