oxycodone hydrochloride

Generic: oxycodone hydrochloride

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

Drug Facts

Product Profile

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

oxycodone hydrochloride 15 mg/1

Manufacturer
Quality Care Products LLC

Identifiers & Regulatory

Product NDC 55700-174
Product ID 55700-174_dd30b87d-7f9b-43b8-b32e-c4d2937d6931
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091393
DEA Schedule cii
Marketing Start 2013-10-18
Marketing End 2027-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700174
Hyphenated Format 55700-174

Supplemental Identifiers

RxCUI
1049611 1049618
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 hydrochloride (source: ndc)
Application Number ANDA091393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (55700-174-30)
  • 60 TABLET in 1 BOTTLE (55700-174-60)
  • 90 TABLET in 1 BOTTLE (55700-174-90)
source: ndc

Packages (3)

55700-174-30 30 TABLET in 1 BOTTLE (55700-174-30) 55700-174-60 60 TABLET in 1 BOTTLE (55700-174-60) 55700-174-90 90 TABLET in 1 BOTTLE (55700-174-90)

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": "dd30b87d-7f9b-43b8-b32e-c4d2937d6931", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618"], "spl_set_id": ["4cadb809-157d-49cc-97b4-3276594f19d2"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55700-174-30)", "package_ndc": "55700-174-30", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55700-174-60)", "package_ndc": "55700-174-60", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-174-90)", "package_ndc": "55700-174-90", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "55700-174_dd30b87d-7f9b-43b8-b32e-c4d2937d6931", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "55700-174", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_end_date": "20270731", "marketing_start_date": "20131018"}