hydromorphone hydrochloride

Generic: hydromorphone hydrochloride

Labeler: padagis us llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name hydromorphone hydrochloride
Generic Name hydromorphone hydrochloride
Labeler padagis us llc
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

hydromorphone hydrochloride 3 mg/1

Manufacturer
Padagis US LLC

Identifiers & Regulatory

Product NDC 0574-7224
Product ID 0574-7224_8c369b50-cf2a-4e30-a31c-ccf5f49ab920
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 1996-01-31

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05747224
Hyphenated Format 0574-7224

Supplemental Identifiers

RxCUI
897749
UNII
L960UP2KRW

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydromorphone hydrochloride (source: ndc)
Generic Name hydromorphone hydrochloride (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 3 mg/1
source: ndc
Packaging
  • 6 PACKET in 1 BOX (0574-7224-06) / 1 SUPPOSITORY in 1 PACKET
source: ndc

Packages (1)

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

Ingredients (1)

hydromorphone hydrochloride (3 mg/1)

Linked Drug Pages (1)

HYDROMORPHONE HYDROCHLORIDE ndc-match (0.9)

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"}