Package 68788-8393-2

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8393-2
Digits Only 6878883932
Product NDC 68788-8393
Product ID 68788-8393_69ab7391-0b01-4bc2-bedb-8959de130500
Description

4 BLISTER PACK in 1 CARTON (68788-8393-2) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-03-01
Brand loperamide hydrochloride
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Loperamide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "69ab7391-0b01-4bc2-bedb-8959de130500", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["5b173bb9-3cca-44ce-9bcb-b9ecc93d3dcf"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (68788-8393-2)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "68788-8393-2", "marketing_start_date": "20230301"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68788-8393_69ab7391-0b01-4bc2-bedb-8959de130500", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68788-8393", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA206548", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}