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 CAPSULE
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-167
Product ID 62559-167_d6bf3c12-70dd-4089-b3ed-0d22371efbd2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205177
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2016-06-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559167
Hyphenated Format 62559-167

Supplemental Identifiers

RxCUI
1049696
UPC
0362559167017
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 ANDA205177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (62559-167-01)
source: ndc

Packages (1)

62559-167-01 100 CAPSULE in 1 BOTTLE (62559-167-01)

Ingredients (1)

oxycodone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6bf3c12-70dd-4089-b3ed-0d22371efbd2", "openfda": {"upc": ["0362559167017"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049696"], "spl_set_id": ["5df92fed-6194-4905-9ef2-9eed0d2e8086"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62559-167-01)", "package_ndc": "62559-167-01", "marketing_start_date": "20160610"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "62559-167_d6bf3c12-70dd-4089-b3ed-0d22371efbd2", "dosage_form": "CAPSULE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "62559-167", "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/1"}], "application_number": "ANDA205177", "marketing_category": "ANDA", "marketing_start_date": "20160610", "listing_expiration_date": "20271231"}