Package 0404-9999-01

Brand: propranolol

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9999-01
Digits Only 0404999901
Product NDC 0404-9999
Product ID 0404-9999_a64c6dcb-7a81-4f7e-bd26-7ca72c56003b
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9999-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2024-07-15
Brand propranolol
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

PROPRANOLOL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a64c6dcb-7a81-4f7e-bd26-7ca72c56003b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["e586996d-9035-4ef4-8c8d-06e70a02577f"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9999-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9999-01", "marketing_start_date": "20240715"}], "brand_name": "PROPRANOLOL", "product_id": "0404-9999_a64c6dcb-7a81-4f7e-bd26-7ca72c56003b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0404-9999", "generic_name": "propranolol hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPRANOLOL", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075826", "marketing_category": "ANDA", "marketing_start_date": "20240715", "listing_expiration_date": "20261231"}