NDC 16729-203

Buspirone Hydrochloride 15 mg tablet

On the label: Accord Healthcare Inc..

Where it's made

Recalls

• Feb 7, 2023 · Class II · Accord Healthcare, Inc.
  CGMP Deviations: recalling drug products following an FDA inspection.
  Lots: Batches: P2105532, Exp. Date 6/30/2024; P2200348, Exp. Date 12/31/2024;
• Feb 7, 2023 · Class II · Accord Healthcare, Inc.
  CGMP Deviations: recalling drug products following an FDA inspection.
  Lots: Batches: a) P2200530, Exp. Date 12/31/2024; b) P2105583, Exp. Date 6/30/2024;
• Feb 7, 2023 · Class II · Accord Healthcare, Inc.
  CGMP Deviations: recalling drug products following an FDA inspection.
  Lots: Batches: P2105483, Exp. Date 7/31/2024;
• Feb 7, 2023 · Class II · Accord Healthcare, Inc.
  CGMP Deviations: recalling drug products following an FDA inspection.
  Lots: Batches: P2105472, Exp. Date 4/30/2024;
• Feb 7, 2023 · Class II · Accord Healthcare, Inc.
  CGMP Deviations: recalling drug products following an FDA inspection.
  Lots: Batches: P2105551, Exp. Date 7/31/2024;

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

Product details

Generic drug

Buspirone: every company that makes it

Form

tablet, oral

Strength

15 mg

Approval

ANDA ANDA202557

On the market since

Dec 15, 2016

Package NDCs

16729-203-01 16729-203-12 16729-203-16 16729-203-17 16729-203-59

Official label

DailyMed (National Library of Medicine), updated Oct 7, 2025

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