oxycodone hydchloride
Generic: oxycodone hydchloride
Labeler: quality care products llcDrug Facts
Product Profile
Brand Name
oxycodone hydchloride
Generic Name
oxycodone hydchloride
Labeler
quality care products llc
Dosage Form
TABLET
Routes
Active Ingredients
oxycodone hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49999-899
Product ID
49999-899_13014be8-5073-42af-b13d-af29c8b906ce
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49999899
Hyphenated Format
49999-899
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (49999-899-15)
- 21 TABLET in 1 BOTTLE (49999-899-21)
- 30 TABLET in 1 BOTTLE (49999-899-30)
- 60 TABLET in 1 BOTTLE (49999-899-60)
- 90 TABLET in 1 BOTTLE (49999-899-90)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13014be8-5073-42af-b13d-af29c8b906ce", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["b9847cc7-67a2-408d-93cf-f9cf420346dd"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (49999-899-15)", "package_ndc": "49999-899-15", "marketing_end_date": "20270630", "marketing_start_date": "20190614"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (49999-899-21)", "package_ndc": "49999-899-21", "marketing_end_date": "20260630", "marketing_start_date": "20190614"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (49999-899-30)", "package_ndc": "49999-899-30", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (49999-899-60)", "package_ndc": "49999-899-60", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (49999-899-90)", "package_ndc": "49999-899-90", "marketing_end_date": "20260630", "marketing_start_date": "20111220"}], "brand_name": "Oxycodone Hydchloride", "product_id": "49999-899_13014be8-5073-42af-b13d-af29c8b906ce", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "49999-899", "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": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_end_date": "20270630", "marketing_start_date": "20111220"}