Package 62559-423-01

Brand: hyoscyamine sulfate

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 62559-423-01
Digits Only 6255942301
Product NDC 62559-423
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-423-01)

Marketing

Marketing Status
Marketed Since 2024-02-15
Brand hyoscyamine sulfate
Generic hyoscyamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f3b6482-bdac-411a-8eee-561674ac224e", "openfda": {"upc": ["0362559423014"], "unii": ["F2R8V82B84"], "rxcui": ["1046770"], "spl_set_id": ["3859133e-88bd-4dd5-90a0-82b64347f1db"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-423-01)", "package_ndc": "62559-423-01", "marketing_start_date": "20240215"}], "brand_name": "Hyoscyamine Sulfate", "product_id": "62559-423_1f3b6482-bdac-411a-8eee-561674ac224e", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "62559-423", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".375 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}