Package 82804-258-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-258-30
Digits Only 8280425830
Product NDC 82804-258
Product ID 82804-258_e289160e-0f3a-4667-b8ba-9c93fbf21a30
Description

30 TABLET in 1 BOTTLE (82804-258-30)

Marketing

Marketing Status
Marketed Since 2025-11-26
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": "e289160e-0f3a-4667-b8ba-9c93fbf21a30", "openfda": {"upc": ["0382804258307"], "unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["e289160e-0f3a-4667-b8ba-9c93fbf21a30"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-258-30)", "package_ndc": "82804-258-30", "marketing_start_date": "20251126"}], "brand_name": "Propranolol Hydrochloride", "product_id": "82804-258_e289160e-0f3a-4667-b8ba-9c93fbf21a30", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-258", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20261231"}