Package 0054-0668-82

Brand: alvimopan

Generic: alvimopan
NDC Package

Package Facts

Identity

Package NDC 0054-0668-82
Digits Only 0054066882
Product NDC 0054-0668
Product ID 0054-0668_89b02f3c-d8da-4b1f-9847-859c4efffabb
Description

6 BLISTER PACK in 1 CARTON (0054-0668-82) / 5 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand alvimopan
Generic alvimopan
Sample Package No

Linked Drug Pages (1)

Alvimopan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "89b02f3c-d8da-4b1f-9847-859c4efffabb", "openfda": {"unii": ["677C126AET"], "rxcui": ["799835"], "spl_set_id": ["59ef406b-79db-4efd-b993-08b937ac682b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0054-0668-82)  / 5 CAPSULE in 1 BLISTER PACK", "package_ndc": "0054-0668-82", "marketing_start_date": "20240206"}], "brand_name": "Alvimopan", "product_id": "0054-0668_89b02f3c-d8da-4b1f-9847-859c4efffabb", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0054-0668", "generic_name": "Alvimopan", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alvimopan", "active_ingredients": [{"name": "ALVIMOPAN", "strength": "12 mg/1"}], "application_number": "ANDA217753", "marketing_category": "ANDA", "marketing_start_date": "20240206", "listing_expiration_date": "20261231"}