Package 72162-1939-1

Brand: hyoscyamine sulfate

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1939-1
Digits Only 7216219391
Product NDC 72162-1939
Description

100 TABLET in 1 BOTTLE (72162-1939-1)

Marketing

Marketing Status
Marketed Since 2023-08-31
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": "51e502c9-5761-4bdf-933b-372169555e69", "openfda": {"unii": ["F2R8V82B84"], "rxcui": ["1047905"], "spl_set_id": ["7258faac-4e08-469b-950c-abe5a5f94445"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1939-1)", "package_ndc": "72162-1939-1", "marketing_start_date": "20230831"}], "brand_name": "Hyoscyamine Sulfate", "product_id": "72162-1939_51e502c9-5761-4bdf-933b-372169555e69", "dosage_form": "TABLET", "product_ndc": "72162-1939", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Bryant Ranch Prepack", "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": "20181001", "listing_expiration_date": "20261231"}