venlafaxine hydrochloride

Product NDC
68788-6424
11-digit product format
687886424
Labeler code
68788
Product ID
68788-6424_17ea8716-6df8-4541-b745-4128b3bdbef1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
venlafaxine hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA090174
Marketing category
ANDA
Marketing start
2016-06-20
Marketing end
0000-00-00
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
75 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-6424-3EA - Each68788-6424fbada38b-e218-4dec-a420-1d34521c21bc12020-05-08
68788-6424-9EA - Each68788-642411baa3dc-b10f-4dec-ae0e-22d79073217312020-05-08

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-6424-168788642401100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-1) 2016-06-200000-00-00NoNoCurrent
68788-6424-26878864240220 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-2) 2016-06-200000-00-00NoNoCurrent
68788-6424-36878864240330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-3) 2016-06-200000-00-00NoNoCurrent
68788-6424-66878864240660 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-6) 2016-06-200000-00-00NoNoCurrent
68788-6424-868788642408120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-8) 2016-06-200000-00-00NoNoCurrent
68788-6424-96878864240990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6424-9) 2016-06-200000-00-00NoNoCurrent