oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: precision dose, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler precision dose, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 15 mg/1

Manufacturer
Precision Dose, Inc.

Identifiers & Regulatory

Product NDC 68094-005
Product ID 68094-005_31203769-a951-4d0c-8d60-4cb7715e26e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203638
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2016-12-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68094005
Hyphenated Format 68094-005

Supplemental Identifiers

RxCUI
1049611
UPC
0368094005616
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 ANDA203638 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (68094-005-61) / 10 TABLET in 1 BLISTER PACK (68094-005-59)
source: ndc

Packages (1)

68094-005-61 10 BLISTER PACK in 1 CARTON (68094-005-61) / 10 TABLET in 1 BLISTER PACK (68094-005-59)

Ingredients (1)

oxycodone hydrochloride (15 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": "31203769-a951-4d0c-8d60-4cb7715e26e8", "openfda": {"upc": ["0368094005616"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["f849c7cc-fa85-47eb-be30-1be137913bf9"], "manufacturer_name": ["Precision Dose, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68094-005-61)  / 10 TABLET in 1 BLISTER PACK (68094-005-59)", "package_ndc": "68094-005-61", "marketing_start_date": "20161221"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "68094-005_31203769-a951-4d0c-8d60-4cb7715e26e8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68094-005", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20161221", "listing_expiration_date": "20261231"}