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
- 72189-175_4c498a8f-f65a-5df5-e063-6394a90ae0fd
- Product NDC
- 72189-175
- Form
- TABLET
- Composition / generic term
- BUSPIRONE HYDROCHLORIDE
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210209
- Source listing expiry
- 20271231
Source-listed ingredients
- BUSPIRONE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (72189-175-30) · 72189-175-30
- 180 TABLET in 1 BOTTLE (72189-175-82) · 72189-175-82
- 90 TABLET in 1 BOTTLE (72189-175-90) · 72189-175-90
Source and coverage
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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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