Felbamate

Product NDC
47781-550
11-digit product format
477810550
Labeler code
47781
Product ID
47781-550_9d9e56d5-39d6-61de-dac9-32f1182ccbe0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
felbamate
Dosage form
TABLET
Route
ORAL
Labeler
Alvogen Inc.
Application
ANDA204595
Marketing category
ANDA
Marketing start
2016-12-28
Marketing end
2020-07-01
Substance
FELBAMATE
Active strength
400 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
47781-550-01EA - Each47781-55066f23e80-8dec-457f-aa60-73601db2678112017-03-06