oxycodone hydrochloride

Generic: oxycodone hydrochloride

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

Drug Facts

Product Profile

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

oxycodone hydrochloride 5 mg/1

Manufacturer
KVK-TECH,INC

Identifiers & Regulatory

Product NDC 10702-018
Product ID 10702-018_31f901b4-04ad-38aa-e063-6294a90ac708
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091393
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2013-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702018
Hyphenated Format 10702-018

Supplemental Identifiers

RxCUI
1049611 1049618 1049621 1049683 1049686
UNII
C1ENJ2TE6C

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 oxycodone hydrochloride (source: ndc)
Generic Name oxycodone hydrochloride (source: ndc)
Application Number ANDA091393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-018-01)
  • 500 TABLET in 1 BOTTLE (10702-018-50)
source: ndc

Packages (2)

10702-018-01 100 TABLET in 1 BOTTLE (10702-018-01) 10702-018-50 500 TABLET in 1 BOTTLE (10702-018-50)

Ingredients (1)

oxycodone hydrochloride (5 mg/1)

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31f901b4-04ad-38aa-e063-6294a90ac708", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["e73897d6-b920-4300-a564-5dbc9c8e9fe9"], "manufacturer_name": ["KVK-TECH,INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-018-01)", "package_ndc": "10702-018-01", "marketing_start_date": "20131018"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-018-50)", "package_ndc": "10702-018-50", "marketing_start_date": "20131018"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "10702-018_31f901b4-04ad-38aa-e063-6294a90ac708", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-018", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "KVK-TECH,INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}