prazosin
Generic: prazosin
Labeler: lannett company, inc.Drug Facts
Product Profile
Brand Name
prazosin
Generic Name
prazosin
Labeler
lannett company, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0527-4182
Product ID
0527-4182_41beba09-90c1-42cc-bfba-ac8a84d09649
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214083
Listing Expiration
2026-12-31
Marketing Start
2024-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05274182
Hyphenated Format
0527-4182
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
prazosin (source: ndc)
Application Number
ANDA214083 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0527-4182-37)
- 250 CAPSULE in 1 BOTTLE (0527-4182-42)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41beba09-90c1-42cc-bfba-ac8a84d09649", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["94021822-60cb-4da6-b809-f565e1d6452d"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0527-4182-37)", "package_ndc": "0527-4182-37", "marketing_start_date": "20240103"}, {"sample": false, "description": "250 CAPSULE in 1 BOTTLE (0527-4182-42)", "package_ndc": "0527-4182-42", "marketing_start_date": "20240103"}], "brand_name": "Prazosin", "product_id": "0527-4182_41beba09-90c1-42cc-bfba-ac8a84d09649", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0527-4182", "generic_name": "Prazosin", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA214083", "marketing_category": "ANDA", "marketing_start_date": "20240103", "listing_expiration_date": "20261231"}