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
- 70954-021_8420b1bd-9aba-43e5-96e1-15ef2342cd12
- Product NDC
- 70954-021
- Form
- CAPSULE
- Composition / generic term
- Prazosin Hydrochloride
- Labeler
- ANI Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181003
- Source listing expiry
- 20271231
Source-listed ingredients
- PRAZOSIN HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (70954-021-10) · 70954-021-10
- 250 CAPSULE in 1 BOTTLE (70954-021-20) · 70954-021-20
- 100 BLISTER PACK in 1 CARTON (70954-021-40) / 1 CAPSULE in 1 BLISTER PACK (70954-021-30) · 70954-021-40
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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