oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: quagen pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler quagen pharmaceuticals llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 100 mg/5mL

Manufacturer
QUAGEN PHARMACEUTICALS LLC

Identifiers & Regulatory

Product NDC 70752-137
Product ID 70752-137_16bbc411-6512-4799-a12d-12b7f3572afe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213761
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2021-06-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70752137
Hyphenated Format 70752-137

Supplemental Identifiers

RxCUI
1049604 1049615
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 ANDA213761 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (70752-137-03) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

70752-137-03 1 BOTTLE in 1 CARTON (70752-137-03) / 30 mL in 1 BOTTLE

Ingredients (1)

oxycodone hydrochloride (100 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": "16bbc411-6512-4799-a12d-12b7f3572afe", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604", "1049615"], "spl_set_id": ["391701e5-2035-43fa-91ce-d27a1af19492"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70752-137-03)  / 30 mL in 1 BOTTLE", "package_ndc": "70752-137-03", "marketing_start_date": "20210602"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "70752-137_16bbc411-6512-4799-a12d-12b7f3572afe", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70752-137", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "100 mg/5mL"}], "application_number": "ANDA213761", "marketing_category": "ANDA", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}