Package 62559-533-01

Brand: propranolol hydrochloride er

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62559-533-01
Digits Only 6255953301
Product NDC 62559-533
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-533-01)

Marketing

Marketing Status
Marketed Since 2017-12-21
Brand propranolol hydrochloride er
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "200aecd3-b441-4856-a9fc-6841ada5489c", "openfda": {"upc": ["0362559531016", "0362559533010", "0362559532013", "0362559530019"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["5415904b-90da-48e8-9f9e-f86749aa129c"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-533-01)", "package_ndc": "62559-533-01", "marketing_start_date": "20171221"}], "brand_name": "Propranolol Hydrochloride ER", "product_id": "62559-533_200aecd3-b441-4856-a9fc-6841ada5489c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62559-533", "generic_name": "propranolol hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "brand_name_suffix": "ER", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "NDA018553", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20171221", "listing_expiration_date": "20261231"}