oxymorphone hydrochloride

Generic: oxymorphone hydrochloride

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

Drug Facts

Product Profile

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

oxymorphone hydrochloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1926
Product ID 63629-1926_c58a9e13-1792-4569-a677-28d9aaf0c9f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210175
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2018-03-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636291926
Hyphenated Format 63629-1926

Supplemental Identifiers

RxCUI
977939
UNII
5Y2EI94NBC

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 oxymorphone hydrochloride (source: ndc)
Generic Name oxymorphone hydrochloride (source: ndc)
Application Number ANDA210175 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63629-1926-1)
source: ndc

Packages (1)

63629-1926-1 100 TABLET in 1 BOTTLE (63629-1926-1)

Ingredients (1)

oxymorphone hydrochloride (5 mg/1)

Linked Drug Pages (1)

OXYMORPHONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c58a9e13-1792-4569-a677-28d9aaf0c9f0", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939"], "spl_set_id": ["560e9425-dfcb-4fb4-a759-b1e3f8f40fdb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1926-1)", "package_ndc": "63629-1926-1", "marketing_start_date": "20210114"}], "brand_name": "OXYMORPHONE HYDROCHLORIDE", "product_id": "63629-1926_c58a9e13-1792-4569-a677-28d9aaf0c9f0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1926", "dea_schedule": "CII", "generic_name": "OXYMORPHONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYMORPHONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210175", "marketing_category": "ANDA", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}