oxycodone hydrochloride
Generic: oxycodone hydrochloride
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
oxycodone hydrochloride
Generic Name
oxycodone hydrochloride
Labeler
redpharm drug
Dosage Form
SOLUTION
Routes
Active Ingredients
oxycodone hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
67296-2167
Product ID
67296-2167_45abe234-8d2e-b01a-e063-6294a90a7789
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA200535
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2013-09-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672962167
Hyphenated Format
67296-2167
Supplemental Identifiers
RxCUI
UPC
UNII
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
NDA200535 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (67296-2167-6) / 60 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45abe234-8d2e-b01a-e063-6294a90a7789", "openfda": {"upc": ["0364950353037", "0364950354058"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["3745020d-df8c-7209-e063-6394a90aabd7"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67296-2167-6) / 60 mL in 1 BOTTLE, PLASTIC", "package_ndc": "67296-2167-6", "marketing_start_date": "20130909"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "67296-2167_45abe234-8d2e-b01a-e063-6294a90a7789", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-2167", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "NDA200535", "marketing_category": "NDA", "marketing_start_date": "20130909", "listing_expiration_date": "20261231"}