Package 67296-2172-1
Brand: loperamide hydrochloride
Generic: loperamide hydrochloridePackage Facts
Identity
Package NDC
67296-2172-1
Digits Only
6729621721
Product NDC
67296-2172
Description
15 CAPSULE in 1 BOTTLE (67296-2172-1)
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": "44f72085-ac64-5dc5-e063-6394a90a0ff0", "openfda": {"upc": ["0359651691014"], "unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["3b0ac1a9-ffa6-9af6-e063-6294a90a2678"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 CAPSULE in 1 BOTTLE (67296-2172-1)", "package_ndc": "67296-2172-1", "marketing_start_date": "20230905"}], "brand_name": "LOPERAMIDE HYDROCHLORIDE", "product_id": "67296-2172_44f72085-ac64-5dc5-e063-6394a90a0ff0", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "67296-2172", "generic_name": "LOPERAMIDE HYDROCHLORIDE", "labeler_name": "Redpharm Drug", "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": "20230905", "listing_expiration_date": "20261231"}