Package 0093-0311-01

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-0311-01
Digits Only 0093031101
Product NDC 0093-0311
Description

100 CAPSULE in 1 BOTTLE (0093-0311-01)

Marketing

Marketing Status
Marketed Since 1993-05-01
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": "863c19d4-c0cd-455e-9a93-5c5157762d02", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["8bf47ac3-746f-47c3-82b2-32ac979ff963"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-0311-01)", "package_ndc": "0093-0311-01", "marketing_start_date": "19930501"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0093-0311-05)", "package_ndc": "0093-0311-05", "marketing_start_date": "19930501"}], "brand_name": "Loperamide Hydrochloride", "product_id": "0093-0311_863c19d4-c0cd-455e-9a93-5c5157762d02", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0093-0311", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA073192", "marketing_category": "ANDA", "marketing_start_date": "19930501", "listing_expiration_date": "20261231"}