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 SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 100 mg/5mL

Manufacturer
KVK-Tech, Inc.

Identifiers & Regulatory

Product NDC 10702-171
Product ID 10702-171_441eb113-64da-ceeb-e063-6394a90a2f74
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208593
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2017-07-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702171
Hyphenated Format 10702-171

Supplemental Identifiers

RxCUI
1049604 1049615
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 ANDA208593 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (10702-171-03) / 30 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

10702-171-03 1 BOTTLE, PLASTIC in 1 CARTON (10702-171-03) / 30 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

oxycodone hydrochloride (100 mg/5mL)

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE, Oxycodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "441eb113-64da-ceeb-e063-6394a90a2f74", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["744f5d1c-7427-492c-8994-c8e817793e53"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (10702-171-03)  / 30 mL in 1 BOTTLE, PLASTIC", "package_ndc": "10702-171-03", "marketing_start_date": "20170721"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "10702-171_441eb113-64da-ceeb-e063-6394a90a2f74", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-171", "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": "100 mg/5mL"}], "application_number": "ANDA208593", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}