Package 72162-1175-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1175-0
Digits Only 7216211750
Product NDC 72162-1175
Description

1000 TABLET in 1 BOTTLE (72162-1175-0)

Marketing

Marketing Status
Marketed Since 2024-10-04
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "088d7e29-6c0b-4377-9c45-f2fa8b58c27d", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["905e205d-4d0b-4ce0-968e-96171164940e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1175-0)", "package_ndc": "72162-1175-0", "marketing_start_date": "20241004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1175-1)", "package_ndc": "72162-1175-1", "marketing_start_date": "20230626"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72162-1175_088d7e29-6c0b-4377-9c45-f2fa8b58c27d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1175", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}