hydromorphone hydrochloride

Generic: hydromorphone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name hydromorphone hydrochloride
Generic Name hydromorphone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydromorphone hydrochloride 2 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-4284
Product ID 63629-4284_07884a78-2a01-453c-870b-7b757b530d22
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA019892
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2009-11-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636294284
Hyphenated Format 63629-4284

Supplemental Identifiers

RxCUI
897696
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)
Application Number NDA019892 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 25 TABLET in 1 BOTTLE (63629-4284-1)
  • 60 TABLET in 1 BOTTLE (63629-4284-2)
  • 30 TABLET in 1 BOTTLE (63629-4284-3)
  • 28 TABLET in 1 BOTTLE (63629-4284-4)
  • 90 TABLET in 1 BOTTLE (63629-4284-5)
  • 120 TABLET in 1 BOTTLE (63629-4284-6)
  • 40 TABLET in 1 BOTTLE (63629-4284-7)
  • 20 TABLET in 1 BOTTLE (63629-4284-8)
  • 10 TABLET in 1 BOTTLE (63629-4284-9)
source: ndc

Packages (9)

63629-4284-1 25 TABLET in 1 BOTTLE (63629-4284-1) 63629-4284-2 60 TABLET in 1 BOTTLE (63629-4284-2) 63629-4284-3 30 TABLET in 1 BOTTLE (63629-4284-3) 63629-4284-4 28 TABLET in 1 BOTTLE (63629-4284-4) 63629-4284-5 90 TABLET in 1 BOTTLE (63629-4284-5) 63629-4284-6 120 TABLET in 1 BOTTLE (63629-4284-6) 63629-4284-7 40 TABLET in 1 BOTTLE (63629-4284-7) 63629-4284-8 20 TABLET in 1 BOTTLE (63629-4284-8) 63629-4284-9 10 TABLET in 1 BOTTLE (63629-4284-9)

Ingredients (1)

hydromorphone hydrochloride (2 mg/1)

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07884a78-2a01-453c-870b-7b757b530d22", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897696"], "spl_set_id": ["2427814c-f32b-8ac5-99b8-5e886fd2d001"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET in 1 BOTTLE (63629-4284-1)", "package_ndc": "63629-4284-1", "marketing_start_date": "20100621"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-4284-2)", "package_ndc": "63629-4284-2", "marketing_start_date": "20110823"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-4284-3)", "package_ndc": "63629-4284-3", "marketing_start_date": "20101022"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (63629-4284-4)", "package_ndc": "63629-4284-4", "marketing_start_date": "20101112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-4284-5)", "package_ndc": "63629-4284-5", "marketing_start_date": "20140611"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-4284-6)", "package_ndc": "63629-4284-6", "marketing_start_date": "20120625"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (63629-4284-7)", "package_ndc": "63629-4284-7", "marketing_start_date": "20140127"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63629-4284-8)", "package_ndc": "63629-4284-8", "marketing_start_date": "20120501"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (63629-4284-9)", "package_ndc": "63629-4284-9", "marketing_start_date": "20200824"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "63629-4284_07884a78-2a01-453c-870b-7b757b530d22", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-4284", "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": "2 mg/1"}], "application_number": "NDA019892", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20091123", "listing_expiration_date": "20261231"}