prazosin

Generic: prazosin

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin
Generic Name prazosin
Labeler lannett company, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 5 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-4182
Product ID 0527-4182_41beba09-90c1-42cc-bfba-ac8a84d09649
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214083
Listing Expiration 2026-12-31
Marketing Start 2024-01-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05274182
Hyphenated Format 0527-4182

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 (source: ndc)
Generic Name prazosin (source: ndc)
Application Number ANDA214083 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0527-4182-37)
  • 250 CAPSULE in 1 BOTTLE (0527-4182-42)
source: ndc

Packages (2)

Ingredients (1)

prazosin hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41beba09-90c1-42cc-bfba-ac8a84d09649", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["94021822-60cb-4da6-b809-f565e1d6452d"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0527-4182-37)", "package_ndc": "0527-4182-37", "marketing_start_date": "20240103"}, {"sample": false, "description": "250 CAPSULE in 1 BOTTLE (0527-4182-42)", "package_ndc": "0527-4182-42", "marketing_start_date": "20240103"}], "brand_name": "Prazosin", "product_id": "0527-4182_41beba09-90c1-42cc-bfba-ac8a84d09649", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0527-4182", "generic_name": "Prazosin", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA214083", "marketing_category": "ANDA", "marketing_start_date": "20240103", "listing_expiration_date": "20261231"}