oxycodone hydrochloride (71930-022)

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 5 mg/5mL

Manufacturer

Eywa Pharma Inc

Identifiers & Regulatory

Product NDC 71930-022

Product ID 71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207511

DEA Schedule cii

Listing Expiration 2027-12-31

Marketing Start 2019-03-01

Pharmacologic Class

Classes

full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71930022

Hyphenated Format 71930-022

Supplemental Identifiers

RxCUI

1049604

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 ANDA207511 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

5 mg/5mL

source: ndc

Packaging

1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLE

source: ndc

Packages (1)

71930-022-43 1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLE

Ingredients (1)

oxycodone hydrochloride (5 mg/5mL)

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "d5dbbf3c-6269-488c-b3a2-9539f45e3945", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["685f409f-946f-4b7e-8130-5ad7b92a5e7a"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71930-022-43)  / 473 mL in 1 BOTTLE", "package_ndc": "71930-022-43", "marketing_start_date": "20190301"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-022", "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": "5 mg/5mL"}], "application_number": "ANDA207511", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20271231"}