Package 62559-422-01

Brand: hyoscyamine sulfate

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 62559-422-01
Digits Only 6255942201
Product NDC 62559-422
Product ID 62559-422_e60b7fbe-fdd5-4932-9f26-cecdeb5c60d5
Description

100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62559-422-01)

Marketing

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

Linked Drug Pages (1)

Hyoscyamine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e60b7fbe-fdd5-4932-9f26-cecdeb5c60d5", "openfda": {"upc": ["0362559422017"], "unii": ["F2R8V82B84"], "rxcui": ["1046985"], "spl_set_id": ["66fdfc33-a7b9-465b-84f1-012cdf5517fd"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62559-422-01)", "package_ndc": "62559-422-01", "marketing_start_date": "20240215"}], "brand_name": "Hyoscyamine Sulfate", "product_id": "62559-422_e60b7fbe-fdd5-4932-9f26-cecdeb5c60d5", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "62559-422", "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": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}