prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55289-536
Product ID
55289-536_41acd2b1-05fc-f6ff-e063-6394a90abda4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072575
Listing Expiration
2026-12-31
Marketing Start
1989-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55289536
Hyphenated Format
55289-536
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
ANDA072575 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-536-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41acd2b1-05fc-f6ff-e063-6394a90abda4", "openfda": {"upc": ["0355289536604"], "unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["e5e129aa-2ee3-4c12-a327-5d5382cf2310"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (55289-536-60)", "package_ndc": "55289-536-60", "marketing_start_date": "19940722"}], "brand_name": "Prazosin Hydrochloride", "product_id": "55289-536_41acd2b1-05fc-f6ff-e063-6394a90abda4", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "55289-536", "generic_name": "prazosin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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": "19890228", "listing_expiration_date": "20261231"}