oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: aurolife pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler aurolife pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 15 mg/1

Manufacturer
Aurolife Pharma, LLC

Identifiers & Regulatory

Product NDC 13107-056
Product ID 13107-056_a06eea3f-6fd5-4b19-9425-4117a488c676
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202160
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2012-07-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13107056
Hyphenated Format 13107-056

Supplemental Identifiers

RxCUI
1049611 1049618 1049621
UPC
0313107055010 0313107056017 0313107057014
UNII
C1ENJ2TE6C

Packaging Origin

Original Packager
true

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 ANDA202160 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (13107-056-01)
  • 30 TABLET in 1 BOTTLE (13107-056-30)
  • 1000 TABLET in 1 BOTTLE (13107-056-99)
source: ndc

Packages (3)

13107-056-01 100 TABLET in 1 BOTTLE (13107-056-01) 13107-056-30 30 TABLET in 1 BOTTLE (13107-056-30) 13107-056-99 1000 TABLET in 1 BOTTLE (13107-056-99)

Ingredients (1)

oxycodone hydrochloride (15 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": "a06eea3f-6fd5-4b19-9425-4117a488c676", "openfda": {"upc": ["0313107055010", "0313107056017", "0313107057014"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621"], "spl_set_id": ["96ad4352-fff3-46a7-85de-466cc161045e"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-056-01)", "package_ndc": "13107-056-01", "marketing_start_date": "20120712"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-056-30)", "package_ndc": "13107-056-30", "marketing_start_date": "20120712"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-056-99)", "package_ndc": "13107-056-99", "marketing_start_date": "20120712"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "13107-056_a06eea3f-6fd5-4b19-9425-4117a488c676", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-056", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202160", "marketing_category": "ANDA", "marketing_start_date": "20120712", "listing_expiration_date": "20261231"}