Package 71610-074-30

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-074-30
Digits Only 7161007430
Product NDC 71610-074
Description

30 TABLET in 1 BOTTLE, PLASTIC (71610-074-30)

Marketing

Marketing Status
Marketed Since 2018-05-21
Brand sotalol hydrochloride
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e87b445-6112-4dfa-9961-95beb8f7eb82", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1922765"], "spl_set_id": ["5ede17b7-3898-4f9f-abec-e15620cef76a"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71610-074-30)", "package_ndc": "71610-074-30", "marketing_start_date": "20180521"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71610-074-60)", "package_ndc": "71610-074-60", "marketing_start_date": "20180521"}], "brand_name": "Sotalol Hydrochloride", "product_id": "71610-074_0e87b445-6112-4dfa-9961-95beb8f7eb82", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "71610-074", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA076214", "marketing_category": "ANDA", "marketing_start_date": "20030909", "listing_expiration_date": "20261231"}