Package 71610-571-60

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-571-60
Digits Only 7161057160
Product NDC 71610-571
Product ID 71610-571_f8a8dd81-4a23-4a7a-9ff5-2684499be0a8
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (71610-571-60)

Marketing

Marketing Status
Marketed Since 2021-06-15
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": "f8a8dd81-4a23-4a7a-9ff5-2684499be0a8", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["5c154cde-0c2f-4215-a6c3-8275cfdf31fe"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (71610-571-60)", "package_ndc": "71610-571-60", "marketing_start_date": "20210615"}], "brand_name": "Prazosin Hydrochloride", "product_id": "71610-571_f8a8dd81-4a23-4a7a-9ff5-2684499be0a8", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71610-571", "generic_name": "prazosin hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19890516", "listing_expiration_date": "20261231"}