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 20 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-613
Product ID 72189-613_323148b2-809b-db11-e063-6294a90abe36
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077712
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2025-04-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189613
Hyphenated Format 72189-613

Supplemental Identifiers

RxCUI
1049686
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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-613-30)
source: ndc

Packages (1)

72189-613-30 30 TABLET in 1 BOTTLE (72189-613-30)

Ingredients (1)

oxycodone hydrochloride (20 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": "323148b2-809b-db11-e063-6294a90abe36", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049686"], "spl_set_id": ["323148b2-809a-db11-e063-6294a90abe36"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-613-30)", "package_ndc": "72189-613-30", "marketing_start_date": "20250407"}], "brand_name": "Oxycodone HCL", "product_id": "72189-613_323148b2-809b-db11-e063-6294a90abe36", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-613", "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": "20 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}