Package 59651-327-01

Brand: phenoxybenzamine hydrochloride

Generic: phenoxybenzamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-327-01
Digits Only 5965132701
Product NDC 59651-327
Product ID 59651-327_3aeb0006-90e3-477a-9c81-0a8a671061d4
Description

100 CAPSULE in 1 BOTTLE (59651-327-01)

Marketing

Marketing Status
Marketed Since 2023-05-08
Brand phenoxybenzamine hydrochloride
Generic phenoxybenzamine hydrochloride
Sample Package No

Linked Drug Pages (1)

PHENOXYBENZAMINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3aeb0006-90e3-477a-9c81-0a8a671061d4", "openfda": {"unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["75f26681-a079-4ff3-9fff-75526041374c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-327-01)", "package_ndc": "59651-327-01", "marketing_start_date": "20230508"}], "brand_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "product_id": "59651-327_3aeb0006-90e3-477a-9c81-0a8a671061d4", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "59651-327", "generic_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENOXYBENZAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENOXYBENZAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215600", "marketing_category": "ANDA", "marketing_start_date": "20230508", "listing_expiration_date": "20261231"}