Package 63868-338-60
Brand: loperamide hydrochloride
Generic: loperamide hydrochloridePackage Facts
Identity
Package NDC
63868-338-60
Digits Only
6386833860
Product NDC
63868-338
Description
60 TABLET in 1 BOTTLE (63868-338-60)
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": "0ea72333-af5b-8141-e063-6294a90afe55", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["237b845b-0f02-410d-9750-c95123e6142d"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BLISTER PACK (63868-338-12)", "package_ndc": "63868-338-12", "marketing_start_date": "19930201"}, {"sample": false, "description": "24 TABLET in 1 BLISTER PACK (63868-338-24)", "package_ndc": "63868-338-24", "marketing_start_date": "19930201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63868-338-60)", "package_ndc": "63868-338-60", "marketing_start_date": "19930201"}], "brand_name": "Loperamide Hydrochloride", "product_id": "63868-338_0ea72333-af5b-8141-e063-6294a90afe55", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63868-338", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Chain Drug Marketing Association 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": "19930201", "listing_expiration_date": "20261231"}