Package 68220-113-50

Brand: Levsin SL

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 68220-113-50
Digits Only 6822011350
Product NDC 68220-113
Description

500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68220-113-50)

Marketing

Marketing Status
Marketed Since 2008-12-01
Brand Levsin SL
Generic hyoscyamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "61809756-6ca7-4ff0-9950-266ddabb39a9", "openfda": {"unii": ["F2R8V82B84"], "rxcui": ["1046982", "1047908"], "spl_set_id": ["f38ece41-b890-11e2-9e96-0800200c9a66"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68220-113-10)", "package_ndc": "68220-113-10", "marketing_start_date": "20081201"}, {"sample": false, "description": "500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68220-113-50)", "package_ndc": "68220-113-50", "marketing_start_date": "20081201"}], "brand_name": "Levsin SL", "product_id": "68220-113_61809756-6ca7-4ff0-9950-266ddabb39a9", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "68220-113", "generic_name": "hyoscyamine sulfate", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levsin", "brand_name_suffix": "SL", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20081201", "listing_expiration_date": "20261231"}