Package 68998-123-24
Brand: loperamide hydrochloride
Generic: loperamide hydrochloridePackage Facts
Identity
Package NDC
68998-123-24
Digits Only
6899812324
Product NDC
68998-123
Description
4 BLISTER PACK in 1 CARTON (68998-123-24) / 6 TABLET in 1 BLISTER PACK
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": "0ea71997-4922-a72e-e063-6294a90a52da", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["01efdce1-25ce-45ff-aeb6-f6fba00e59aa"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (68998-123-24) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "68998-123-24", "marketing_start_date": "20180501"}], "brand_name": "Loperamide Hydrochloride", "product_id": "68998-123_0ea71997-4922-a72e-e063-6294a90a52da", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68998-123", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Marc Glassman, Inc.", "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": "20180501", "listing_expiration_date": "20261231"}