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NDC 61919-0882-30 DESVENLAFAXINE ER 50 mg/1 Details

DESVENLAFAXINE ER 50 mg/1

DESVENLAFAXINE ER is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Direct_Rx. The primary component is DESVENLAFAXINE SUCCINATE.

MedlinePlus Drug Summary

Desvenlafaxine is used to treat depression. Desvenlafaxine is in a class of medications called selective serotonin and norepinephrine reuptake inhibitors (SNRIs). It works by increasing the amounts of serotonin and norepinephrine, natural substances in the brain that help maintain mental balance.

Related Packages: 61919-0882-30
Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Desvenlafaxine

Product Information

NDC	61919-0882
Product ID	61919-882_0e9cb2cf-9a08-48f6-e063-6294a90a3acc
Associated GPIs	58180020207520
GCN Sequence Number	063736
GCN Sequence Number Description	desvenlafaxine succinate TAB ER 24H 50 MG ORAL
HIC3	H7C
HIC3 Description	SEROTONIN-NOREPINEPHRINE REUPTAKE-INHIB (SNRIS)
GCN	99451
HICL Sequence Number	035420
HICL Sequence Number Description	DESVENLAFAXINE SUCCINATE
Brand/Generic	Generic
Proprietary Name	DESVENLAFAXINE ER
Proprietary Name Suffix	n/a
Non-Proprietary Name	DESVENLAFAXINE ER
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	50
Active Ingredient Units	mg/1
Substance Name	DESVENLAFAXINE SUCCINATE
Labeler Name	Direct_Rx
Pharmaceutical Class	Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA204172
Listing Certified Through	2025-12-31

Package

NDC 61919-0882-30 (61919088230)

Pricing Information	N/A
NDC Package Code	61919-882-30
Billing NDC	61919088230
Package	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-882-30)
Marketing Start Date	2019-06-04
NDC Exclude Flag	N