oxycodone hydrochloride

Generic: oxycodone

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6966
Product ID 0904-6966_9059237f-b963-405f-8988-4f50981a4260
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203638
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2012-10-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046966
Hyphenated Format 0904-6966

Supplemental Identifiers

RxCUI
1049611 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 hydrochloride (source: ndc)
Generic Name oxycodone (source: ndc)
Application Number ANDA203638 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6966-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6966-61 100 BLISTER PACK in 1 CARTON (0904-6966-61) / 1 TABLET in 1 BLISTER PACK

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": "9059237f-b963-405f-8988-4f50981a4260", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049621"], "spl_set_id": ["6b6db42b-9821-4aa6-8566-297037d84079"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6966-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6966-61", "marketing_start_date": "20121030"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "0904-6966_9059237f-b963-405f-8988-4f50981a4260", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-6966", "dea_schedule": "CII", "generic_name": "Oxycodone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}