Package 72789-372-90

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-372-90
Digits Only 7278937290
Product NDC 72789-372
Product ID 72789-372_3cf820d7-b455-5342-e063-6394a90a4f78
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-372-90)

Marketing

Marketing Status
Marketed Since 2024-01-22
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": "3cf820d7-b455-5342-e063-6394a90a4f78", "openfda": {"upc": ["0372789372907"], "unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["95a2eacd-b6b7-4e92-ae14-52fbee6c6543"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-372-90)", "package_ndc": "72789-372-90", "marketing_start_date": "20240122"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72789-372_3cf820d7-b455-5342-e063-6394a90a4f78", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-372", "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": "40 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}