Package 63323-604-01

Brand: propranolol

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-604-01
Digits Only 6332360401
Product NDC 63323-604
Description

10 VIAL, SINGLE-DOSE in 1 TRAY (63323-604-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2001-09-07
Brand propranolol
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "505851c4-b18c-4cd7-805c-4e923cc1fa7e", "openfda": {"upc": ["0363323604004"], "unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["f14ea537-dd5c-4c78-9037-9a85e9e610ef"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (63323-604-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-604-01", "marketing_start_date": "20010907"}], "brand_name": "Propranolol", "product_id": "63323-604_505851c4-b18c-4cd7-805c-4e923cc1fa7e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63323-604", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "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": "20010907", "listing_expiration_date": "20261231"}