Desvenlafaxine — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

DESVENLAFAXINE SUCCINATE

Base moiety

DESVENLAFAXINE

RxNorm CUI

1607617

UNII

ZB22ENF0XR

Medication products

14

Brand names

5

Dosage forms

3

FAERS reports

26,841 · not a risk measure

Products containing this ingredient

Source: NDC Directory 14 products

Desvenlafaxine Tablet, Film Coated, Extended Release
Rx ANDA 7 NDC
Desvenlafaxine Powder
1 NDC
DESVENLAFAXINE ER Desvenlafaxine Er · Tablet, Film Coated, Extended Release
Rx ANDA TE AB 1 NDC
Desvenlafaxine ER Tablet, Extended Release
Rx ANDA TE AB 1 NDC
Desvenlafaxine Succinate Powder
9 NDC
Desvenlafaxine Succinate (Process-II) Powder
1 NDC
DESVENLAFAXINE SUCCINATE MONOHYDRATE Desvenlafaxine Succinate Monohydrate · Powder
1 NDC
O-DESMETHYL VENLAFAXINE FUMARATE O-Desmethyl Venlafaxine Fumarate · Powder
1 NDC
O-Desmethyl Venlafaxine Succinate Powder
1 NDC
o-desvenlafaxine succinate Powder
1 NDC
Desvenlafaxine Tablet, Extended Release
Rx ANDA TE AB 1 recall 45 NDC
desvenlafaxine succinate Tablet, Extended Release
ANDA TE AB 5 NDC
Desvenlafaxine Succinate Tablet, Film Coated, Extended Release
Rx ANDA TE AB 9 NDC
Pristiq desvenlafaxine succinate · Tablet, Extended Release
Rx NDA TE AB 1 recall 3 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	7	Desvenlafaxine, Desvenlafaxine Succinate, Desvenlafaxine Succinate (Process-II), DESVENLAFAXINE SUCCINATE MONOHYDRATE …
TABLET, Extended Release	4	Desvenlafaxine ER, Desvenlafaxine, desvenlafaxine succinate, Pristiq
TABLET, Film COATED, Extended Release	3	Desvenlafaxine, DESVENLAFAXINE ER, Desvenlafaxine Succinate

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals