Package 72162-1178-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1178-1
Digits Only 7216211781
Product NDC 72162-1178
Product ID 72162-1178_215b3a31-7efd-4b68-82ca-a6b8f3e8b1fb
Description

100 TABLET in 1 BOTTLE (72162-1178-1)

Marketing

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

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "215b3a31-7efd-4b68-82ca-a6b8f3e8b1fb", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856556"], "spl_set_id": ["8c681a79-bf2c-4eea-9b81-140ddba00616"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1178-1)", "package_ndc": "72162-1178-1", "marketing_start_date": "20241004"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72162-1178_215b3a31-7efd-4b68-82ca-a6b8f3e8b1fb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1178", "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": "60 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}