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
- 72205-275_486d4f26-60ae-4e6c-aa36-0b298a7f9aed
- Product NDC
- 72205-275
- Form
- CAPSULE
- Composition / generic term
- prazosin hydrochloride
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240917
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAZOSIN HYDROCHLORIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 BOTTLE (72205-275-90) · 72205-275-90
- 100 CAPSULE in 1 BOTTLE (72205-275-91) · 72205-275-91
- 250 CAPSULE in 1 BOTTLE (72205-275-95) · 72205-275-95
- 1000 CAPSULE in 1 BOTTLE (72205-275-99) · 72205-275-99
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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