oxycodone hydrochloride

Generic: oxycodone hydrochloride

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

Drug Facts

Product Profile

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

oxycodone hydrochloride 5 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-0425
Product ID 67296-0425_3252751e-38fb-6056-e063-6394a90a1340
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076758
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2009-07-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672960425
Hyphenated Format 67296-0425

Supplemental Identifiers

RxCUI
1049621
UPC
0367296042542
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 ANDA076758 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (67296-0425-1)
  • 4 TABLET in 1 BOTTLE (67296-0425-4)
source: ndc

Packages (2)

67296-0425-1 20 TABLET in 1 BOTTLE (67296-0425-1) 67296-0425-4 4 TABLET in 1 BOTTLE (67296-0425-4)

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": "3252751e-38fb-6056-e063-6394a90a1340", "openfda": {"upc": ["0367296042542"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["92614a3a-331d-16ad-e053-2a95a90a47cc"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-0425-1)", "package_ndc": "67296-0425-1", "marketing_start_date": "20190101"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE (67296-0425-4)", "package_ndc": "67296-0425-4", "marketing_start_date": "20190101"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "67296-0425_3252751e-38fb-6056-e063-6394a90a1340", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-0425", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076758", "marketing_category": "ANDA", "marketing_start_date": "20090730", "listing_expiration_date": "20261231"}