oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

oxycodone hydrochloride 5 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3600
Product ID 68071-3600_17f796b6-3f89-c988-e063-6394a90a7cb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091393
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2013-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713600
Hyphenated Format 68071-3600

Supplemental Identifiers

RxCUI
1049621
UPC
0368071360042
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 ANDA091393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 4 TABLET in 1 BOTTLE (68071-3600-4)
source: ndc

Packages (1)

Ingredients (1)

oxycodone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "17f796b6-3f89-c988-e063-6394a90a7cb8", "openfda": {"upc": ["0368071360042"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["17f7946d-e889-b736-e063-6394a90a42e0"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (68071-3600-4)", "package_ndc": "68071-3600-4", "marketing_start_date": "20240508"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "68071-3600_17f796b6-3f89-c988-e063-6394a90a7cb8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-3600", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}