Package 59651-272-01

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-272-01
Digits Only 5965127201
Product NDC 59651-272
Description

100 CAPSULE in 1 BOTTLE (59651-272-01)

Marketing

Marketing Status
Marketed Since 2023-03-31
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08114092-fa12-4f58-b08e-03cadf9f726b", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["08114092-fa12-4f58-b08e-03cadf9f726b"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-272-01)", "package_ndc": "59651-272-01", "marketing_start_date": "20230331"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (59651-272-99)", "package_ndc": "59651-272-99", "marketing_start_date": "20230331"}], "brand_name": "Prazosin Hydrochloride", "product_id": "59651-272_08114092-fa12-4f58-b08e-03cadf9f726b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "59651-272", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA213052", "marketing_category": "ANDA", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}