prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler mylan institutional inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 1 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-630
Product ID 51079-630_3a874e40-912d-740d-e063-6394a90a4778
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072575
Listing Expiration 2026-12-31
Marketing Start 1998-10-05

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079630
Hyphenated Format 51079-630

Supplemental Identifiers

RxCUI
198141 312593 312594
UNII
X0Z7454B90

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prazosin hydrochloride (source: ndc)
Generic Name prazosin hydrochloride (source: ndc)
Application Number ANDA072575 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-630-20) / 1 CAPSULE in 1 BLISTER PACK (51079-630-01)
source: ndc

Packages (1)

Ingredients (1)

prazosin hydrochloride (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a874e40-912d-740d-e063-6394a90a4778", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["e6a029b2-802f-4cc5-8795-20e177e8d779"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-630-20)  / 1 CAPSULE in 1 BLISTER PACK (51079-630-01)", "package_ndc": "51079-630-20", "marketing_start_date": "19981005"}], "brand_name": "Prazosin Hydrochloride", "product_id": "51079-630_3a874e40-912d-740d-e063-6394a90a4778", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "51079-630", "generic_name": "prazosin hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19981005", "listing_expiration_date": "20261231"}