Venlafaxine Hydrochloride

Product NDC
13811-713
11-digit product format
138110713
Labeler code
13811
Product ID
13811-713_55564637-0e7a-4684-be84-9d8c4cecacc3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
venlafaxine hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Trigen Laboratories, LLC
Application
NDA022104
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2010-04-29
Marketing end
2026-05-31
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
Current FDA listing
Yes

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
17db3736-056c-48b9-b0f4-00fccabb14e6Product name520251118
7be8b949-f2c0-bdd8-e89d-8af92c1b2eadProduct name920250224
b1435b59-059c-404b-a587-53656bf80e17Product name120230314
6005cd75-f7b1-d6be-3cb5-4bd30d5c4617Product name320190314

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13811-713-30Venlafaxine Hydrochloride30 in 1 BOTTLETABLET, EXTENDED RELEASE3014
13811-713-90Venlafaxine Hydrochloride90 in 1 BOTTLETABLET, EXTENDED RELEASE9014

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
13811-713-30EA - Each13811-7135c1105c6-62c2-4f49-9be3-81afd875732a12016-12-07
13811-713-90EA - Each13811-7137ca1e4fb-e286-46b1-857b-fc7d1ff7933512016-12-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13811-713VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [TRIGEN LABORATORIES, LLC]11Current NDC, Legacy NDC, 2 package rows20240606_fdaed1c2-dd0a-4bf3-975a-86fe3e7f0c97.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
808744venlafaxine HCl 150 MG 24HR Extended Release Oral TabletPSNfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808748venlafaxine HCl 225 MG 24HR Extended Release Oral TabletPSNfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808751venlafaxine HCl 37.5 MG 24HR Extended Release Oral TabletPSNfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808753venlafaxine HCl 75 MG 24HR Extended Release Oral TabletPSNfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
80874424 HR venlafaxine 150 MG Extended Release Oral TabletSCDfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
80874824 HR venlafaxine 225 MG Extended Release Oral TabletSCDfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
80875124 HR venlafaxine 37.5 MG Extended Release Oral TabletSCDfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
80875324 HR venlafaxine 75 MG Extended Release Oral TabletSCDfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808744venlafaxine 150 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808744venlafaxine 150 MG 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808748venlafaxine 225 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808748venlafaxine 225 MG 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808751venlafaxine 37.5 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808751venlafaxine 37.5 MG 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808753venlafaxine 75 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714
808753venlafaxine 75 MG 24 HR Extended Release Oral TabletSYfdaed1c2-dd0a-4bf3-975a-86fe3e7f0c9714

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
13811-713-301381107133030 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-713-30) 2010-04-292026-05-31NoNoCurrent
13811-713-901381107139090 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-713-90) 2010-04-292026-05-31NoNoCurrent