ONGENTYS

Product NDC
70370-3050
11-digit product format
703703050
Labeler code
70370
Product ID
70370-3050_62cbc1fe-da3b-436f-ba28-5dca7becb528
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
opicapone
Dosage form
CAPSULE
Route
ORAL
Labeler
Neurocrine Biosciences, Inc.
Application
NDA212489
Marketing category
NDA
Marketing start
2020-04-24
Marketing end
0000-00-00
Substance
OPICAPONE
Active strength
50 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70370-3050-27037030500230 CAPSULE in 1 BOTTLE (70370-3050-2) 30 capsule2020-04-240000-00-00NoNoCurrent