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 CAPSULE
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
KVK-TECH, INC.

Identifiers & Regulatory

Product NDC 10702-023
Product ID 10702-023_437f25fb-bd72-c6d8-e063-6294a90a42d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202773
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-08-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702023
Hyphenated Format 10702-023

Supplemental Identifiers

RxCUI
1049696
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 ANDA202773 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (10702-023-01)
  • 60 CAPSULE in 1 BOTTLE (10702-023-06)
source: ndc

Packages (2)

10702-023-01 100 CAPSULE in 1 BOTTLE (10702-023-01) 10702-023-06 60 CAPSULE in 1 BOTTLE (10702-023-06)

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": "437f25fb-bd72-c6d8-e063-6294a90a42d7", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049696"], "spl_set_id": ["338b5391-e5f7-40a2-8b15-57f47cbc4813"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (10702-023-01)", "package_ndc": "10702-023-01", "marketing_start_date": "20150820"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (10702-023-06)", "package_ndc": "10702-023-06", "marketing_start_date": "20150820"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "10702-023_437f25fb-bd72-c6d8-e063-6294a90a42d7", "dosage_form": "CAPSULE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-023", "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": "ANDA202773", "marketing_category": "ANDA", "marketing_start_date": "20150820", "listing_expiration_date": "20261231"}