Package 68016-123-97
Brand: loperamide hydrochloride
Generic: loperamide hydrochloridePackage Facts
Identity
Package NDC
68016-123-97
Digits Only
6801612397
Product NDC
68016-123
Description
96 TABLET in 1 BOTTLE (68016-123-97)
Marketing
Marketing Status
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": "0ea714a1-b048-bc87-e063-6294a90a28e7", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["b070896b-1e22-41d4-a66d-8d3be1699217"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BLISTER PACK (68016-123-06)", "package_ndc": "68016-123-06", "marketing_start_date": "19930201"}, {"sample": false, "description": "18 TABLET in 1 BLISTER PACK (68016-123-18)", "package_ndc": "68016-123-18", "marketing_start_date": "19930201"}, {"sample": false, "description": "24 TABLET in 1 BLISTER PACK (68016-123-24)", "package_ndc": "68016-123-24", "marketing_start_date": "19930201"}, {"sample": false, "description": "96 TABLET in 1 BOTTLE (68016-123-97)", "package_ndc": "68016-123-97", "marketing_start_date": "19930201"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68016-123_0ea714a1-b048-bc87-e063-6294a90a28e7", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68016-123", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA074091", "marketing_category": "ANDA", "marketing_start_date": "19930201", "listing_expiration_date": "20261231"}