Package 68084-654-01

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-654-01
Digits Only 6808465401
Product NDC 68084-654
Product ID 68084-654_18aceadd-5a62-1d75-e063-6394a90ab39a
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-654-01) / 1 TABLET in 1 BLISTER PACK (68084-654-11)

Marketing

Marketing Status
Marketed Since 2014-03-11
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": ["ORAL"], "spl_id": "18aceadd-5a62-1d75-e063-6394a90ab39a", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923426"], "spl_set_id": ["4614480b-b36e-4dbd-9fc0-d083890d297d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-654-01)  / 1 TABLET in 1 BLISTER PACK (68084-654-11)", "package_ndc": "68084-654-01", "marketing_start_date": "20140311"}], "brand_name": "Sotalol Hydrochloride", "product_id": "68084-654_18aceadd-5a62-1d75-e063-6394a90ab39a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "68084-654", "generic_name": "Sotalol Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA076140", "marketing_category": "ANDA", "marketing_start_date": "20140311", "listing_expiration_date": "20261231"}