oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler redpharm drug
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/5mL

Manufacturer
Redpharm Drug

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
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962167
Hyphenated Format 67296-2167

Supplemental Identifiers

RxCUI
1049604
UPC
0364950353037 0364950354058
UNII
C1ENJ2TE6C

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (67296-2167-6) / 60 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

oxycodone hydrochloride (5 mg/5mL)

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"}