United States · FDA National Drug Code directory
Paroxetine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 13107-154_c399d3cd-13a5-4493-9a93-c4bf5e2532fc
- Product NDC
- 13107-154
- Form
- TABLET, FILM COATED
- Composition / generic term
- Paroxetine
- Labeler
- Aurolife Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091203
- Source listing expiry
- 20261231
Source-listed ingredients
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01) · 13107-154-01
- 500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05) · 13107-154-05
- 30 TABLET, FILM COATED in 1 BOTTLE (13107-154-30) · 13107-154-30
- 90 TABLET, FILM COATED in 1 BOTTLE (13107-154-90) · 13107-154-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99) · 13107-154-99
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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