venlafaxine

Product NDC
68788-7586
11-digit product format
687887586
Labeler code
68788
Product ID
68788-7586_1c3a258b-9ea5-4b36-9069-991f793e66b7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
venlafaxine
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA078932
Marketing category
ANDA
Marketing start
2020-02-11
Marketing end
0000-00-00
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
25 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
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7586-1EA - Each68788-75865e3be296-a745-4388-a639-9f266dff021a12020-04-20
68788-7586-3EA - Each68788-7586d0072701-f3b1-432a-b508-f7671af303ef12020-04-20
68788-7586-6EA - Each68788-7586b6e8c6b7-5a2d-4e38-92bc-9699eca853fc12020-04-20
68788-7586-9EA - Each68788-7586916c00ac-69d9-42f7-aa42-0362fd121c3f12020-04-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7586-168788758601100 TABLET in 1 BOTTLE (68788-7586-1) 100 tablet2020-02-110000-00-00NoNoCurrent
68788-7586-36878875860330 TABLET in 1 BOTTLE (68788-7586-3) 30 tablet2020-02-110000-00-00NoNoCurrent
68788-7586-66878875860660 TABLET in 1 BOTTLE (68788-7586-6) 60 tablet2020-02-110000-00-00NoNoCurrent
68788-7586-96878875860990 TABLET in 1 BOTTLE (68788-7586-9) 90 tablet2020-02-110000-00-00NoNoCurrent