Package 35573-473-02

Brand: phenoxybenzamine hydrochloride

Generic: phenoxybenzamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 35573-473-02
Digits Only 3557347302
Product NDC 35573-473
Description

100 CAPSULE in 1 BOTTLE (35573-473-02)

Marketing

Marketing Status
Marketed Since 2023-05-08
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": "609aa41e-4cb5-4cdf-9137-f429c21b4fab", "openfda": {"unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["609aa41e-4cb5-4cdf-9137-f429c21b4fab"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (35573-473-02)", "package_ndc": "35573-473-02", "marketing_start_date": "20230508"}], "brand_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "product_id": "35573-473_609aa41e-4cb5-4cdf-9137-f429c21b4fab", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "35573-473", "generic_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "labeler_name": "Burel Pharmaceuticals, LLC", "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"}