Paroxetine Hydrochloride Hemihydrate — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

Base moiety

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

RxNorm CUI

1738803

UNII

X2ELS050D8

Medication products

8

Brand names

3

Dosage forms

4

FAERS reports

41,814 · not a risk measure

Products containing this ingredient

Source: NDC Directory 8 products

Paroxetine Suspension
Rx ANDA TE AB 1 NDC
Paroxetine Hydrochloride Powder
2 NDC
paroxetine hydrochloride (hemihydrate) Powder
3 NDC
Paroxetine Hydrochloride Hemihydrate Powder
11 NDC
Paroxetine Tablet, Film Coated, Extended Release
Rx ANDA TE AB 1 recall 21 NDC
Paroxetine Tablet, Film Coated
Rx ANDA TE AB 10 recalls 119 NDC
Paroxetine Hydrochloride Tablet, Film Coated, Extended Release
Rx ANDA TE AB 7 NDC
paroxetine hydrochloride Tablet, Film Coated
Rx ANDA TE AB 8 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	3	Paroxetine Hydrochloride, paroxetine hydrochloride (hemihydrate), Paroxetine Hydrochloride Hemihydrate
TABLET, Film COATED, Extended Release	2	Paroxetine, Paroxetine Hydrochloride
TABLET, Film Coated	2	Paroxetine, paroxetine hydrochloride
Suspension	1	Paroxetine

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