Package 51525-0115-1

Brand: hyoscyamine er

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 51525-0115-1
Digits Only 5152501151
Product NDC 51525-0115
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51525-0115-1)

Marketing

Marketing Status
Marketed Since 2016-05-01
Brand hyoscyamine er
Generic hyoscyamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0522d7a7-0349-48e2-85d9-827963cc4986", "openfda": {"upc": ["0351525011515"], "unii": ["F2R8V82B84"], "rxcui": ["1046770"], "spl_set_id": ["5bbce8c0-a9c9-45b9-8457-1542bd3d9449"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51525-0115-1)", "package_ndc": "51525-0115-1", "marketing_start_date": "20160501"}], "brand_name": "Hyoscyamine ER", "product_id": "51525-0115_0522d7a7-0349-48e2-85d9-827963cc4986", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "51525-0115", "generic_name": "hyoscyamine sulfate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine", "brand_name_suffix": "ER", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".375 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160501", "listing_expiration_date": "20261231"}