oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler bryant ranch prepack
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/5mL

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1749
Product ID 72162-1749_acd2a06e-f3f7-4aef-85b3-e17d651eac28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204979
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-10-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621749
Hyphenated Format 72162-1749

Supplemental Identifiers

RxCUI
1049604
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 ANDA204979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (72162-1749-2) / 473 mL in 1 BOTTLE
source: ndc

Packages (1)

72162-1749-2 1 BOTTLE in 1 CARTON (72162-1749-2) / 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": "acd2a06e-f3f7-4aef-85b3-e17d651eac28", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["e84ea009-3cab-4721-bd21-1123eccce515"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72162-1749-2)  / 473 mL in 1 BOTTLE", "package_ndc": "72162-1749-2", "marketing_start_date": "20151013"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1749_acd2a06e-f3f7-4aef-85b3-e17d651eac28", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1749", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA204979", "marketing_category": "ANDA", "marketing_start_date": "20151013", "listing_expiration_date": "20261231"}