oxycodone hydrochloride

Generic: oxycodone hydrochloride

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

Drug Facts

Product Profile

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

oxycodone hydrochloride 5 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2188
Product ID 67296-2188_44f3146e-88e3-80e1-e063-6394a90a3a28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077712
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2024-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962188
Hyphenated Format 67296-2188

Supplemental Identifiers

RxCUI
1049621
UPC
0364380262015 0364380260011 0364380259015 0364380261018 0364380263012
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 ANDA077712 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)
source: ndc

Packages (1)

67296-2188-1 12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)

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": "44f3146e-88e3-80e1-e063-6394a90a3a28", "openfda": {"upc": ["0364380262015", "0364380260011", "0364380259015", "0364380261018", "0364380263012"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["439c2de6-3ea5-e829-e063-6294a90aa77d"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)", "package_ndc": "67296-2188-1", "marketing_start_date": "20240910"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "67296-2188_44f3146e-88e3-80e1-e063-6394a90a3a28", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-2188", "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/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20261231"}