Package 16477-738-01

Brand: hyoscyamine sulfate

Generic: hyoscyamine sulfate
NDC Package

Package Facts

Identity

Package NDC 16477-738-01
Digits Only 1647773801
Product NDC 16477-738
Product ID 16477-738_415c6bd6-14f7-8049-e063-6294a90a2f5f
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16477-738-01)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "415c6bd6-14f7-8049-e063-6294a90a2f5f", "openfda": {"upc": ["0316477738019"], "unii": ["F2R8V82B84"], "rxcui": ["1046770"], "spl_set_id": ["b12f856f-7157-4aee-bf73-1fdcb4834ffc"], "manufacturer_name": ["Laser Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16477-738-01)", "package_ndc": "16477-738-01", "marketing_start_date": "20240126"}], "brand_name": "Hyoscyamine Sulfate", "product_id": "16477-738_415c6bd6-14f7-8049-e063-6294a90a2f5f", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "16477-738", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Laser Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".375 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240126", "listing_expiration_date": "20261231"}