prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-089
Product ID
82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215697
Listing Expiration
2026-12-31
Marketing Start
2023-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804089
Hyphenated Format
82804-089
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA215697 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (82804-089-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a928735-179f-4637-8c4e-3b5e01d45bf2", "openfda": {"upc": ["0382804089901"], "unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["2a928735-179f-4637-8c4e-3b5e01d45bf2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (82804-089-90)", "package_ndc": "82804-089-90", "marketing_start_date": "20240314"}], "brand_name": "prazosin hydrochloride", "product_id": "82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "82804-089", "generic_name": "prazosin hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}