Package 72789-495-90

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-495-90
Digits Only 7278949590
Product NDC 72789-495
Product ID 72789-495_308b44b0-6f25-7151-e063-6394a90a7ccc
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-495-90)

Marketing

Marketing Status
Marketed Since 2025-03-17
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": "308b44b0-6f25-7151-e063-6394a90a7ccc", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["85973689-bb21-483f-becb-c5c8bfb05658"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-495-90)", "package_ndc": "72789-495-90", "marketing_start_date": "20250317"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72789-495_308b44b0-6f25-7151-e063-6394a90a7ccc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-495", "generic_name": "Propranolol Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20191031", "listing_expiration_date": "20261231"}