Package 72603-229-01

Brand: phenoxybenzamine hydrochloride

Generic: phenoxybenzamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-229-01
Digits Only 7260322901
Product NDC 72603-229
Product ID 72603-229_26f154d8-7509-4ed1-b9f4-4359987af757
Description

100 CAPSULE in 1 BOTTLE (72603-229-01)

Marketing

Marketing Status
Marketed Since 2024-10-01
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": "26f154d8-7509-4ed1-b9f4-4359987af757", "openfda": {"unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["48a047c0-f409-420b-990a-2cab953a96cd"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72603-229-01)", "package_ndc": "72603-229-01", "marketing_start_date": "20241001"}], "brand_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "product_id": "72603-229_26f154d8-7509-4ed1-b9f4-4359987af757", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72603-229", "generic_name": "PHENOXYBENZAMINE HYDROCHLORIDE", "labeler_name": "NorthStar Rx 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": "20241001", "listing_expiration_date": "20261231"}