Paroxetine Hydrochloride 37.5 mg tablet, film coated, extended release

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.

Recalls

• Sep 23, 2026 · Class II · Apotex Corp.
  Failed dissolution specifications.
  Lots: Lot# TY9495, Exp Date: 05/2027.
• Mar 24, 2014 · Class II · Apotex Inc.
  Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.
  Lots: Lot # 2A001, Exp. 01/15 Lot # 2A002, Exp. 01/15 Lot # 2C003, Exp. 03/15 Lot # 2F005, Exp. 06/15 Lot # 2G006, Exp. 07/15
• Mar 24, 2014 · Class II · Apotex Inc.
  Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.
  Lots: Lot # 2A002, Exp. 01/15 Lot # 2A003, Exp. 01/15 Lot # 2C004, Exp. 03/15 Lot # 2C005, Exp. 03/15 Lot # 2E008, Exp. 05/15 Lot # 2F009, Exp. 06/15 Lot # 2F010, Exp. 06/15 Lot # 2H011, Exp. 08/15 Lot # 2H012, Exp. 08/15 Lot # 2H013, Exp. 0815
• Mar 24, 2014 · Class II · Apotex Inc.
  Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.
  Lots: Lot # 2C002, Exp. 03/15 Lot # 2H004, Exp. 08/15 Lot # 2H006, Exp. 08/15

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Paroxetine: every company that makes it

Form

tablet, film coated, extended release, oral

Strength

37.5 mg

Approval

NDA authorized generic NDA020936

On the market since

Aug 9, 2019

Package NDCs

60505-1318-3

Official label

DailyMed (National Library of Medicine), updated Sep 16, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?