prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 2 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-272
Product ID 59651-272_08114092-fa12-4f58-b08e-03cadf9f726b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213052
Listing Expiration 2026-12-31
Marketing Start 2023-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651272
Hyphenated Format 59651-272

Supplemental Identifiers

RxCUI
198141 312593 312594
UNII
X0Z7454B90

Packaging Origin

Original Packager
true

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 ANDA213052 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (59651-272-01)
  • 1000 CAPSULE in 1 BOTTLE (59651-272-99)
source: ndc

Packages (2)

59651-272-01 100 CAPSULE in 1 BOTTLE (59651-272-01) 59651-272-99 1000 CAPSULE in 1 BOTTLE (59651-272-99)

Ingredients (1)

prazosin hydrochloride (2 mg/1)

Linked Drug Pages (1)

Prazosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08114092-fa12-4f58-b08e-03cadf9f726b", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["08114092-fa12-4f58-b08e-03cadf9f726b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-272-01)", "package_ndc": "59651-272-01", "marketing_start_date": "20230331"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (59651-272-99)", "package_ndc": "59651-272-99", "marketing_start_date": "20230331"}], "brand_name": "Prazosin Hydrochloride", "product_id": "59651-272_08114092-fa12-4f58-b08e-03cadf9f726b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "59651-272", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA213052", "marketing_category": "ANDA", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}