oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: eywa pharma inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler eywa pharma inc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 20 mg/mL

Manufacturer
Eywa Pharma Inc

Identifiers & Regulatory

Product NDC 71930-023
Product ID 71930-023_353e35c4-e3fa-46d0-8497-8872b8c53c39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209897
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2018-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71930023
Hyphenated Format 71930-023

Supplemental Identifiers

RxCUI
1049615
UPC
0371930023309
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 ANDA209897 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (71930-023-30) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

71930-023-30 1 BOTTLE in 1 CARTON (71930-023-30) / 30 mL in 1 BOTTLE

Ingredients (1)

oxycodone hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "353e35c4-e3fa-46d0-8497-8872b8c53c39", "openfda": {"upc": ["0371930023309"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049615"], "spl_set_id": ["c801963d-f54d-4ed5-82c4-8b278528d3dc"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71930-023-30)  / 30 mL in 1 BOTTLE", "package_ndc": "71930-023-30", "marketing_start_date": "20180601"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71930-023_353e35c4-e3fa-46d0-8497-8872b8c53c39", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-023", "dea_schedule": "CII", "generic_name": "Oxycodone hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA209897", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20271231"}