Package 0574-7224-06

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0574-7224-06
Digits Only 0574722406
Product NDC 0574-7224
Product ID 0574-7224_8c369b50-cf2a-4e30-a31c-ccf5f49ab920
Description

6 PACKET in 1 BOX (0574-7224-06) / 1 SUPPOSITORY in 1 PACKET

Marketing

Marketing Status
Marketed Since 1996-01-31
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": ["RECTAL"], "spl_id": "8c369b50-cf2a-4e30-a31c-ccf5f49ab920", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897749"], "spl_set_id": ["1bfbba46-1979-4797-a29e-d67718131686"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 BOX (0574-7224-06)  / 1 SUPPOSITORY in 1 PACKET", "package_ndc": "0574-7224-06", "marketing_start_date": "19960131"}], "brand_name": "HYDROMORPHONE HYDROCHLORIDE", "product_id": "0574-7224_8c369b50-cf2a-4e30-a31c-ccf5f49ab920", "dosage_form": "SUPPOSITORY", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0574-7224", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROMORPHONE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "3 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19960131", "listing_expiration_date": "20261231"}