Package 0054-0386-63

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-0386-63
Digits Only 0054038663
Product NDC 0054-0386
Product ID 0054-0386_4c3c8198-731d-4136-9222-01063f3364cb
Description

473 mL in 1 BOTTLE (0054-0386-63)

Marketing

Marketing Status
Marketed Since 2012-03-01
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c3c8198-731d-4136-9222-01063f3364cb", "openfda": {"upc": ["0300540386634"], "unii": ["L960UP2KRW"], "rxcui": ["897657", "897702", "897710"], "spl_set_id": ["cc574063-6ede-4da7-82c4-7450c92b229b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0054-0386-63)", "package_ndc": "0054-0386-63", "marketing_start_date": "20120301"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0054-0386_4c3c8198-731d-4136-9222-01063f3364cb", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0386", "dea_schedule": "CII", "generic_name": "hydromorphone hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA074653", "marketing_category": "ANDA", "marketing_start_date": "20120301", "listing_expiration_date": "20271231"}