hydromorphone hydrochloride

Generic: hydromorphone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name hydromorphone hydrochloride
Generic Name hydromorphone hydrochloride
Labeler bryant ranch prepack
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

hydromorphone hydrochloride 3 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-2532
Product ID 63629-2532_971f9f4c-1e16-40fb-b08f-e5dc1424e2d2
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 636292532
Hyphenated Format 63629-2532

Supplemental Identifiers

RxCUI
897749
UNII
L960UP2KRW

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 (63629-2532-1) / 1 SUPPOSITORY in 1 PACKET
source: ndc

Packages (1)

Ingredients (1)

hydromorphone hydrochloride (3 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "971f9f4c-1e16-40fb-b08f-e5dc1424e2d2", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897749"], "spl_set_id": ["bec32a94-4b79-4bd4-b000-45e9030d3106"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 BOX (63629-2532-1)  / 1 SUPPOSITORY in 1 PACKET", "package_ndc": "63629-2532-1", "marketing_start_date": "20210428"}], "brand_name": "HYDROMORPHONE HYDROCHLORIDE", "product_id": "63629-2532_971f9f4c-1e16-40fb-b08f-e5dc1424e2d2", "dosage_form": "SUPPOSITORY", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2532", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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"}