oxycodone hcl

Generic: oxycodone hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hcl
Generic Name oxycodone hcl
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-618
Product ID 72189-618_3a851e5a-f061-4676-e063-6294a90ac16c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077712
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2025-04-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189618
Hyphenated Format 72189-618

Supplemental Identifiers

RxCUI
1049621
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 hcl (source: ndc)
Generic Name oxycodone hcl (source: ndc)
Application Number ANDA077712 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-618-30)
  • 60 TABLET in 1 BOTTLE (72189-618-60)
source: ndc

Packages (2)

72189-618-30 30 TABLET in 1 BOTTLE (72189-618-30) 72189-618-60 60 TABLET in 1 BOTTLE (72189-618-60)

Ingredients (1)

oxycodone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Oxycodone HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a851e5a-f061-4676-e063-6294a90ac16c", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["3245cd2f-8ad0-b755-e063-6394a90a603c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-618-30)", "package_ndc": "72189-618-30", "marketing_start_date": "20250408"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-618-60)", "package_ndc": "72189-618-60", "marketing_start_date": "20250408"}], "brand_name": "Oxycodone HCL", "product_id": "72189-618_3a851e5a-f061-4676-e063-6294a90ac16c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-618", "dea_schedule": "CII", "generic_name": "Oxycodone HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone HCL", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}