Package 69367-678-01

Brand: hyoscyamine sulfate sl

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 69367-678-01
Digits Only 6936767801
Product NDC 69367-678
Description

100 TABLET in 1 BOTTLE (69367-678-01)

Marketing

Marketing Status
Marketed Since 2025-04-02
Brand hyoscyamine sulfate 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": "1c473f01-dccd-4be7-bb0b-9a028f90fd22", "openfda": {"unii": ["F2R8V82B84"], "rxcui": ["1046982"], "spl_set_id": ["2b7d1604-3e95-4fc9-a65d-2c06ace16009"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-678-01)", "package_ndc": "69367-678-01", "marketing_start_date": "20250402"}], "brand_name": "Hyoscyamine Sulfate SL", "product_id": "69367-678_1c473f01-dccd-4be7-bb0b-9a028f90fd22", "dosage_form": "TABLET", "product_ndc": "69367-678", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate", "brand_name_suffix": "SL", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250402", "listing_expiration_date": "20261231"}