oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler ani pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/5mL

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-151
Product ID 62559-151_2dd00699-5e0a-42cd-8b52-0d8025d37d39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204979
DEA Schedule cii
Listing Expiration 2027-12-31
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 62559151
Hyphenated Format 62559-151

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 ANDA204979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (62559-151-16) / 473 mL in 1 BOTTLE
source: ndc

Packages (1)

62559-151-16 1 BOTTLE in 1 CARTON (62559-151-16) / 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": "2dd00699-5e0a-42cd-8b52-0d8025d37d39", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["819ed9fc-0a21-4ed0-9080-91912c5f8ce2"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (62559-151-16)  / 473 mL in 1 BOTTLE", "package_ndc": "62559-151-16", "marketing_start_date": "20151013"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "62559-151_2dd00699-5e0a-42cd-8b52-0d8025d37d39", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "62559-151", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "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": "20271231"}