oxymorphone hydrochloride

Generic: oxymorphone hydrochloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxymorphone hydrochloride
Generic Name oxymorphone hydrochloride
Labeler kvk-tech, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxymorphone hydrochloride 5 mg/1

Manufacturer
KVK-Tech, Inc.

Identifiers & Regulatory

Product NDC 10702-070
Product ID 10702-070_499ffc26-7516-aea3-e063-6394a90a5845
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203601
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2013-02-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702070
Hyphenated Format 10702-070

Supplemental Identifiers

RxCUI
977939 977942
UNII
5Y2EI94NBC

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 oxymorphone hydrochloride (source: ndc)
Generic Name oxymorphone hydrochloride (source: ndc)
Application Number ANDA203601 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-070-01)
  • 60 TABLET in 1 BOTTLE (10702-070-06)
source: ndc

Packages (2)

10702-070-01 100 TABLET in 1 BOTTLE (10702-070-01) 10702-070-06 60 TABLET in 1 BOTTLE (10702-070-06)

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": "499ffc26-7516-aea3-e063-6394a90a5845", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["dcb5b5d2-7d0a-497a-8f1e-3b96fd43320b"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-070-01)", "package_ndc": "10702-070-01", "marketing_start_date": "20130211"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-070-06)", "package_ndc": "10702-070-06", "marketing_start_date": "20180625"}], "brand_name": "Oxymorphone Hydrochloride", "product_id": "10702-070_499ffc26-7516-aea3-e063-6394a90a5845", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-070", "dea_schedule": "CII", "generic_name": "Oxymorphone Hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone Hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203601", "marketing_category": "ANDA", "marketing_start_date": "20130211", "listing_expiration_date": "20271231"}