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Active ingredient

Prazosin

111 finished FDA listings contain Prazosin as their only active ingredient.

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FDA NDC Directory

Ingredient names as written by FDA
PRAZOSIN HYDROCHLORIDE
Dosage forms
Capsule
Routes
Oral
Manufacturers / labelers
34
Strengths listed
1 mg/1 · 2 mg/1 · 5 mg/1

RxNorm (National Library of Medicine)

Ingredient concept RxCUI 8629

Drugs@FDA applications

Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.

ApplicationSponsorOriginal approvalListings
NDA 017442PFIZER1976-06-234
ANDA 071745TEVA PHARMS1988-09-1212
ANDA 072575MYLAN1989-02-2814
ANDA 210971NOVITIUM PHARMA2018-10-0322
ANDA 214608GRANULES2021-12-239
ANDA 213406APPCO2022-10-215
ANDA 215697MANKIND PHARMA2022-12-3023
ANDA 217268ALEMBIC2023-03-066
ANDA 213052AUROBINDO PHARMA LTD2023-03-318
ANDA 214083LANNETT CO INC2024-01-033
ANDA 216727MSN2024-09-175

Official labeling on DailyMed

Showing the 12 most recent of 70 labels.

Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.