Levetiracetam

Product NDC
35356-621
11-digit product format
353560621
Labeler code
35356
Product ID
35356-621_c2ee9978-f68f-44b2-9756-c4893e571d47
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Eire Medical & Surgical Supply DBA Quality Care Products LLC
Application
ANDA078154
Marketing category
ANDA
Marketing start
2011-11-14
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
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
44YRR34555LEVETIRACETAM102767-28-2LEVETIRACETAM