Package 0615-8497-39

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8497-39
Digits Only 0615849739
Product NDC 0615-8497
Description

30 CAPSULE in 1 BLISTER PACK (0615-8497-39)

Marketing

Marketing Status
Marketed Since 2024-01-12
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": "96819325-1225-4982-8e6a-85b217a6b6d8", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["f245e8f4-e06e-492e-8c46-af1fce1633fc"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (0615-8497-39)", "package_ndc": "0615-8497-39", "marketing_start_date": "20240112"}], "brand_name": "Loperamide Hydrochloride", "product_id": "0615-8497_96819325-1225-4982-8e6a-85b217a6b6d8", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0615-8497", "generic_name": "Loperamide Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA216876", "marketing_category": "ANDA", "marketing_start_date": "20230126", "listing_expiration_date": "20261231"}