Package 72603-328-02

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-328-02
Digits Only 7260332802
Product NDC 72603-328
Description

500 CAPSULE in 1 BOTTLE (72603-328-02)

Marketing

Marketing Status
Marketed Since 2024-12-01
Brand loperamide hydrochloride
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "858c2b62-98e6-46d7-9253-9b3a00040a4e", "openfda": {"upc": ["0372603328011"], "unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["858c2b62-98e6-46d7-9253-9b3a00040a4e"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72603-328-01)", "package_ndc": "72603-328-01", "marketing_start_date": "20241201"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72603-328-02)", "package_ndc": "72603-328-02", "marketing_start_date": "20241201"}], "brand_name": "LOPERAMIDE HYDROCHLORIDE", "product_id": "72603-328_858c2b62-98e6-46d7-9253-9b3a00040a4e", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72603-328", "generic_name": "LOPERAMIDE HYDROCHLORIDE", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOPERAMIDE HYDROCHLORIDE", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA218122", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}