United States · FDA National Drug Code directory
Prazosin 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
- 59651-273_08114092-fa12-4f58-b08e-03cadf9f726b
- Product NDC
- 59651-273
- Form
- CAPSULE
- Composition / generic term
- Prazosin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230331
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAZOSIN HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (59651-273-01) · 59651-273-01
- 250 CAPSULE in 1 BOTTLE (59651-273-25) · 59651-273-25
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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