Effexor

Product NDC
67544-189
11-digit product format
675440189
Labeler code
67544
Product ID
67544-189_d6e1473b-b1ff-4562-b1ab-65e820de2692
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
venlafaxine hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, Inc.
Application
NDA020699
Marketing category
NDA
Marketing start
1997-11-01
Marketing end
0000-00-00
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67544-189-53EA - Each67544-189d8044656-48aa-4624-ad5d-2fbc3c2ca9ad12013-02-13