Package 69724-112-10

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69724-112-10
Digits Only 6972411210
Product NDC 69724-112
Product ID 69724-112_d155f318-ecbf-4392-90a1-4409c5b8d13f
Description

1 VIAL in 1 CARTON (69724-112-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2015-10-15
Brand sotalol hydrochloride
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Sotalol hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d155f318-ecbf-4392-90a1-4409c5b8d13f", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["904630"], "spl_set_id": ["ff3061ab-d930-4318-a5be-684e38be229e"], "manufacturer_name": ["ALTATHERA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (69724-112-10)  / 10 mL in 1 VIAL", "package_ndc": "69724-112-10", "marketing_start_date": "20151015"}], "brand_name": "Sotalol hydrochloride", "product_id": "69724-112_d155f318-ecbf-4392-90a1-4409c5b8d13f", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "69724-112", "generic_name": "Sotalol hydrochloride", "labeler_name": "ALTATHERA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "15 mg/mL"}], "application_number": "NDA022306", "marketing_category": "NDA", "marketing_start_date": "20151015", "listing_expiration_date": "20261231"}