ROWEEPRA

Product NDC
69102-103
11-digit product format
691020103
Labeler code
69102
Product ID
69102-103_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
1000 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
69102-103-01EA - Each69102-10388f3ed53-a049-4696-a2c5-16a77a70c97012017-05-04