United States · FDA National Drug Code directory

Buspirone Hydrochloride

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
80425-0303_2a9c0c91-2b32-4def-e063-6294a90a58ef
Product NDC
80425-0303
Form
TABLET
Composition / generic term
Buspirone Hydrochloride
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20230406
Source listing expiry
20261231

Source-listed ingredients

  • BUSPIRONE HYDROCHLORIDE — 15 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (80425-0303-1) · 80425-0303-1
  • 60 TABLET in 1 BOTTLE (80425-0303-2) · 80425-0303-2
  • 90 TABLET in 1 BOTTLE (80425-0303-3) · 80425-0303-3

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →