Package 69367-677-01

Brand: hyoscyamine sulfate

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 69367-677-01
Digits Only 6936767701
Product NDC 69367-677
Product ID 69367-677_7f632295-ea1b-4ef3-ad00-34bcc84e6cb3
Description

100 TABLET in 1 BOTTLE (69367-677-01)

Marketing

Marketing Status
Marketed Since 2025-04-02
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": "7f632295-ea1b-4ef3-ad00-34bcc84e6cb3", "openfda": {"upc": ["0369367677011"], "unii": ["F2R8V82B84"], "rxcui": ["1047905"], "spl_set_id": ["9c0ae67b-7887-4820-ad77-8ea7261f9ed3"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-677-01)", "package_ndc": "69367-677-01", "marketing_start_date": "20250402"}], "brand_name": "Hyoscyamine Sulfate", "product_id": "69367-677_7f632295-ea1b-4ef3-ad00-34bcc84e6cb3", "dosage_form": "TABLET", "product_ndc": "69367-677", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Westminster Pharmaceuticals, LLC", "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": "20250402", "listing_expiration_date": "20261231"}