Package 60219-1502-1

Brand: phenoxybenzamine hydrochloride

Generic: phenoxybenzamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60219-1502-1
Digits Only 6021915021
Product NDC 60219-1502
Description

100 CAPSULE in 1 BOTTLE (60219-1502-1)

Marketing

Marketing Status
Marketed Since 2020-10-30
Brand phenoxybenzamine hydrochloride
Generic phenoxybenzamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f872082d-e917-4945-9cd8-59c082cd32d8", "openfda": {"unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["0be6a394-cd10-42fc-97cf-ad53d81d8d93"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (60219-1502-1)", "package_ndc": "60219-1502-1", "marketing_start_date": "20201030"}], "brand_name": "Phenoxybenzamine hydrochloride", "product_id": "60219-1502_f872082d-e917-4945-9cd8-59c082cd32d8", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60219-1502", "generic_name": "Phenoxybenzamine hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenoxybenzamine hydrochloride", "active_ingredients": [{"name": "PHENOXYBENZAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212568", "marketing_category": "ANDA", "marketing_start_date": "20201030", "listing_expiration_date": "20261231"}