Package 82804-089-90

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-089-90
Digits Only 8280408990
Product NDC 82804-089
Product ID 82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2
Description

90 CAPSULE in 1 BOTTLE (82804-089-90)

Marketing

Marketing Status
Marketed Since 2024-03-14
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (1)

prazosin hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a928735-179f-4637-8c4e-3b5e01d45bf2", "openfda": {"upc": ["0382804089901"], "unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["2a928735-179f-4637-8c4e-3b5e01d45bf2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (82804-089-90)", "package_ndc": "82804-089-90", "marketing_start_date": "20240314"}], "brand_name": "prazosin hydrochloride", "product_id": "82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "82804-089", "generic_name": "prazosin hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}