prazosin hydrochloride

Generic: prazosin hydrochloride

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

Drug Facts

Product Profile

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

prazosin hydrochloride 2 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-2302
Product ID 0378-2302_96e4be0d-95bb-44e6-bbfd-55d6694a2e02
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 03782302
Hyphenated Format 0378-2302

Supplemental Identifiers

RxCUI
198141 312593 312594
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 ANDA072575 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-01)
  • 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-10)
source: ndc

Packages (2)

0378-2302-01 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-01) 0378-2302-10 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-10)

Ingredients (1)

prazosin hydrochloride (2 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": "96e4be0d-95bb-44e6-bbfd-55d6694a2e02", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["1ce90aaf-d075-4617-9a47-e8d922096d23"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-01)", "package_ndc": "0378-2302-01", "marketing_start_date": "19890228"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-10)", "package_ndc": "0378-2302-10", "marketing_start_date": "19890228"}], "brand_name": "Prazosin Hydrochloride", "product_id": "0378-2302_96e4be0d-95bb-44e6-bbfd-55d6694a2e02", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0378-2302", "generic_name": "prazosin hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19890228", "listing_expiration_date": "20261231"}