Venlafaxine hydrochloride

Product NDC
80425-0297
11-digit product format
804250297
Labeler code
80425
Product ID
80425-0297_2a9ba8f4-6ced-e827-e063-6394a90a0300
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Venlafaxine hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA200834
Marketing category
ANDA
Marketing start
2023-04-10
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
150 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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7D7RX5A8MOVENLAFAXINE HYDROCHLORIDE99300-78-4VENLAFAXINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
80425-0297-18042502970130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0297-1) 2023-04-10NoNoHistorical
80425-0297-28042502970260 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0297-2) 2023-04-10NoNoHistorical
80425-0297-38042502970390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0297-3) 2023-04-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Venlafaxine HCL ER CapsuleAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2