prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 1 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7335
Product ID 68788-7335_aa35a037-4e75-4d98-8aee-7863c3055d48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071745
Listing Expiration 2026-12-31
Marketing Start 2019-03-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887335
Hyphenated Format 68788-7335

Supplemental Identifiers

RxCUI
312593
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 ANDA071745 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (68788-7335-1)
  • 30 CAPSULE in 1 BOTTLE (68788-7335-3)
  • 60 CAPSULE in 1 BOTTLE (68788-7335-6)
  • 90 CAPSULE in 1 BOTTLE (68788-7335-9)
source: ndc

Packages (4)

68788-7335-1 100 CAPSULE in 1 BOTTLE (68788-7335-1) 68788-7335-3 30 CAPSULE in 1 BOTTLE (68788-7335-3) 68788-7335-6 60 CAPSULE in 1 BOTTLE (68788-7335-6) 68788-7335-9 90 CAPSULE in 1 BOTTLE (68788-7335-9)

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": "aa35a037-4e75-4d98-8aee-7863c3055d48", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["c8202658-422f-41db-bdee-7bb95b972b32"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68788-7335-1)", "package_ndc": "68788-7335-1", "marketing_start_date": "20190312"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7335-3)", "package_ndc": "68788-7335-3", "marketing_start_date": "20190312"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68788-7335-6)", "package_ndc": "68788-7335-6", "marketing_start_date": "20190312"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68788-7335-9)", "package_ndc": "68788-7335-9", "marketing_start_date": "20190312"}], "brand_name": "Prazosin Hydrochloride", "product_id": "68788-7335_aa35a037-4e75-4d98-8aee-7863c3055d48", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7335", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA071745", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}