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: 68071-3336_1cd71696-d959-be3e-e063-6394a90a28c8
Product NDC: 68071-3336
Form: TABLET
Composition / generic term: Buspirone Hydrochloride
Labeler: NuCare Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20161215
Source listing expiry: 20261231

Source-listed ingredients

BUSPIRONE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (68071-3336-3) · 68071-3336-3
60 TABLET in 1 BOTTLE (68071-3336-6) · 68071-3336-6
90 TABLET in 1 BOTTLE (68071-3336-9) · 68071-3336-9

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 →