oxycodone hydchloride

Generic: oxycodone hydchloride

Labeler: quality care products llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydchloride
Generic Name oxycodone hydchloride
Labeler quality care products llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 10 mg/1

Manufacturer
Quality Care Products LLC

Identifiers & Regulatory

Product NDC 35356-839
Product ID 35356-839_d1220dd0-8ab8-47f6-9da9-e22ea724cda0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091393
DEA Schedule cii
Marketing Start 2011-12-20
Marketing End 2027-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 35356839
Hyphenated Format 35356-839

Supplemental Identifiers

RxCUI
1049683
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 hydchloride (source: ndc)
Generic Name oxycodone hydchloride (source: ndc)
Application Number ANDA091393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (35356-839-30)
  • 60 TABLET in 1 BOTTLE (35356-839-60)
  • 90 TABLET in 1 BOTTLE (35356-839-90)
source: ndc

Packages (3)

35356-839-30 30 TABLET in 1 BOTTLE (35356-839-30) 35356-839-60 60 TABLET in 1 BOTTLE (35356-839-60) 35356-839-90 90 TABLET in 1 BOTTLE (35356-839-90)

Ingredients (1)

oxycodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Oxycodone Hydchloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d1220dd0-8ab8-47f6-9da9-e22ea724cda0", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049683"], "spl_set_id": ["28156b13-0ba9-4dc4-be24-9c3070a7e1cc"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (35356-839-30)", "package_ndc": "35356-839-30", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (35356-839-60)", "package_ndc": "35356-839-60", "marketing_end_date": "20270630", "marketing_start_date": "20210430"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (35356-839-90)", "package_ndc": "35356-839-90", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}], "brand_name": "Oxycodone Hydchloride", "product_id": "35356-839_d1220dd0-8ab8-47f6-9da9-e22ea724cda0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "35356-839", "dea_schedule": "CII", "generic_name": "Oxycodone Hydchloride", "labeler_name": "Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydchloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}