Desvenlafaxine Succinate

Product NDC
68788-7488
11-digit product format
687887488
Labeler code
68788
Product ID
68788-7488_ef9c2990-b917-413b-a994-51643ead21c9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desvenlafaxine Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA204172
Marketing category
ANDA
Marketing start
2020-04-30
Marketing end
0000-00-00
Substance
DESVENLAFAXINE SUCCINATE
Active strength
100 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7488-168788748801100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7488-1) 2020-04-300000-00-00NoNoCurrent
68788-7488-36878874880330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7488-3) 2020-04-300000-00-00NoNoCurrent
68788-7488-66878874880660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7488-6) 2020-04-300000-00-00NoNoCurrent
68788-7488-96878874880990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7488-9) 2020-04-300000-00-00NoNoCurrent