Package 0615-8520-39

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8520-39
Digits Only 0615852039
Product NDC 0615-8520
Description

30 CAPSULE in 1 BLISTER PACK (0615-8520-39)

Marketing

Marketing Status
Marketed Since 2024-08-13
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": "86d3c997-3449-46f4-8bc9-1805c5255e04", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593", "312594"], "spl_set_id": ["511b4409-7273-4b74-ae55-47c97f0c3ea4"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (0615-8520-39)", "package_ndc": "0615-8520-39", "marketing_start_date": "20240813"}], "brand_name": "Prazosin Hydrochloride", "product_id": "0615-8520_86d3c997-3449-46f4-8bc9-1805c5255e04", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0615-8520", "generic_name": "Prazosin Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA210971", "marketing_category": "ANDA", "marketing_start_date": "20181003", "listing_expiration_date": "20261231"}