oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: novel laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler novel laboratories, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
Novel Laboratories, Inc.

Identifiers & Regulatory

Product NDC 40032-950
Product ID 40032-950_65077bf1-49cf-4205-91f6-d6e2e81281ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204752
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-08-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 40032950
Hyphenated Format 40032-950

Supplemental Identifiers

RxCUI
1049696
UPC
0340032950035 0340032950011
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 ANDA204752 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (40032-950-01)
  • 30 CAPSULE in 1 BOTTLE (40032-950-03)
  • 500 CAPSULE in 1 BOTTLE (40032-950-50)
source: ndc

Packages (3)

40032-950-01 100 CAPSULE in 1 BOTTLE (40032-950-01) 40032-950-03 30 CAPSULE in 1 BOTTLE (40032-950-03) 40032-950-50 500 CAPSULE in 1 BOTTLE (40032-950-50)

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": "65077bf1-49cf-4205-91f6-d6e2e81281ce", "openfda": {"upc": ["0340032950035", "0340032950011"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049696"], "spl_set_id": ["69410bf3-0d3a-41f9-b10a-c4ee3770f728"], "manufacturer_name": ["Novel Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (40032-950-01)", "package_ndc": "40032-950-01", "marketing_start_date": "20150824"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (40032-950-03)", "package_ndc": "40032-950-03", "marketing_start_date": "20150824"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (40032-950-50)", "package_ndc": "40032-950-50", "marketing_start_date": "20150824"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "40032-950_65077bf1-49cf-4205-91f6-d6e2e81281ce", "dosage_form": "CAPSULE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "40032-950", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Novel Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA204752", "marketing_category": "ANDA", "marketing_start_date": "20150824", "listing_expiration_date": "20261231"}