Package 0093-1061-01

Brand: sotalol hydrochloride

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-1061-01
Digits Only 0093106101
Product NDC 0093-1061
Description

100 TABLET in 1 BOTTLE (0093-1061-01)

Marketing

Marketing Status
Marketed Since 2000-05-04
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": "b0c7f185-187e-443c-9ca8-7ff9658bf713", "openfda": {"upc": ["0300931062017", "0300931060013", "0300931063014", "0300931061010"], "unii": ["HEC37C70XX"], "rxcui": ["904589", "1923422", "1923424", "1923426"], "spl_set_id": ["8e2772cb-7dea-42d1-ba31-d479ba7cb09a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-1061-01)", "package_ndc": "0093-1061-01", "marketing_start_date": "20000504"}], "brand_name": "Sotalol Hydrochloride", "product_id": "0093-1061_b0c7f185-187e-443c-9ca8-7ff9658bf713", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "0093-1061", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol Hydrochloride", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA075429", "marketing_category": "ANDA", "marketing_start_date": "20000504", "listing_expiration_date": "20261231"}