Package 71610-814-27

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-814-27
Digits Only 7161081427
Product NDC 71610-814
Description

1250 CAPSULE in 1 BOTTLE (71610-814-27)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "1547c4d1-e65a-275c-e063-6294a90a8329", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["15479b91-add3-e5dd-e063-6294a90ac15a"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1250 CAPSULE in 1 BOTTLE (71610-814-27)", "package_ndc": "71610-814-27", "marketing_start_date": "20240403"}], "brand_name": "Prazosin Hydrochloride", "product_id": "71610-814_1547c4d1-e65a-275c-e063-6294a90a8329", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71610-814", "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": "5 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19890516", "listing_expiration_date": "20261231"}