prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler novadoz pharmaceuticals llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 1 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-275
Product ID 72205-275_486d4f26-60ae-4e6c-aa36-0b298a7f9aed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216727
Listing Expiration 2026-12-31
Marketing Start 2024-09-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205275
Hyphenated Format 72205-275

Supplemental Identifiers

RxCUI
198141 312593 312594
UPC
0372205277991 0372205275997 0372205276956 0372205275911 0372205275904 0372205277953 0372205276994 0372205275959 0372205276918 0372205277915
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 ANDA216727 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (72205-275-90)
  • 100 CAPSULE in 1 BOTTLE (72205-275-91)
  • 250 CAPSULE in 1 BOTTLE (72205-275-95)
  • 1000 CAPSULE in 1 BOTTLE (72205-275-99)
source: ndc

Packages (4)

72205-275-90 90 CAPSULE in 1 BOTTLE (72205-275-90) 72205-275-91 100 CAPSULE in 1 BOTTLE (72205-275-91) 72205-275-95 250 CAPSULE in 1 BOTTLE (72205-275-95) 72205-275-99 1000 CAPSULE in 1 BOTTLE (72205-275-99)

Ingredients (1)

prazosin hydrochloride (1 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": "486d4f26-60ae-4e6c-aa36-0b298a7f9aed", "openfda": {"upc": ["0372205277991", "0372205275997", "0372205276956", "0372205275911", "0372205275904", "0372205277953", "0372205276994", "0372205275959", "0372205276918", "0372205277915"], "unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["486d4f26-60ae-4e6c-aa36-0b298a7f9aed"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72205-275-90)", "package_ndc": "72205-275-90", "marketing_start_date": "20250416"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72205-275-91)", "package_ndc": "72205-275-91", "marketing_start_date": "20250416"}, {"sample": false, "description": "250 CAPSULE in 1 BOTTLE (72205-275-95)", "package_ndc": "72205-275-95", "marketing_start_date": "20250416"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72205-275-99)", "package_ndc": "72205-275-99", "marketing_start_date": "20250416"}], "brand_name": "prazosin hydrochloride", "product_id": "72205-275_486d4f26-60ae-4e6c-aa36-0b298a7f9aed", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72205-275", "generic_name": "prazosin hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA216727", "marketing_category": "ANDA", "marketing_start_date": "20240917", "listing_expiration_date": "20261231"}