prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55289536
Hyphenated Format 55289-536

Supplemental Identifiers

RxCUI
312593
UPC
0355289536604
UNII
X0Z7454B90

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-536-60)
source: ndc

Packages (1)

Ingredients (1)

prazosin hydrochloride (1 mg/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"}