Package 69367-679-01

Brand: hyoscyamine sulfate odt

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 69367-679-01
Digits Only 6936767901
Product NDC 69367-679
Product ID 69367-679_d40f28c0-8358-4b25-a957-568e01125dfe
Description

100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)

Marketing

Marketing Status
Marketed Since 2025-04-02
Brand hyoscyamine sulfate odt
Generic hyoscyamine sulfate
Sample Package No

Linked Drug Pages (1)

Hyoscyamine Sulfate ODT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d40f28c0-8358-4b25-a957-568e01125dfe", "openfda": {"upc": ["0369367679015"], "unii": ["F2R8V82B84"], "rxcui": ["1046985"], "spl_set_id": ["9429898d-301f-4ebc-8b1d-60595f76f1e3"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)", "package_ndc": "69367-679-01", "marketing_start_date": "20250402"}], "brand_name": "Hyoscyamine Sulfate ODT", "product_id": "69367-679_d40f28c0-8358-4b25-a957-568e01125dfe", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "69367-679", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate", "brand_name_suffix": "ODT", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250402", "listing_expiration_date": "20261231"}