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
71205-280_b02f563b-a2cb-42f8-932c-8e307467a300
Product NDC
71205-280
Form
TABLET
Composition / generic term
BusPIRone Hydrochloride
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20180703
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 (71205-280-30) · 71205-280-30
  • 60 TABLET in 1 BOTTLE (71205-280-60) · 71205-280-60
  • 90 TABLET in 1 BOTTLE (71205-280-90) · 71205-280-90

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.

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BusPIRone Hydrochloride — United States | Molindra Medicines