oxycodone hydrochloride

Generic: oxycodone hydrochloride

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

Drug Facts

Product Profile

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

oxycodone hydrochloride 5 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2368
Product ID 68071-2368_4b455e52-2501-d55a-e063-6294a90a7ba6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202160
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2012-07-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712368
Hyphenated Format 68071-2368

Supplemental Identifiers

RxCUI
1049621
UPC
0368071236866
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 ANDA202160 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE (68071-2368-6)
source: ndc

Packages (1)

68071-2368-6 6 TABLET in 1 BOTTLE (68071-2368-6)

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": "4b455e52-2501-d55a-e063-6294a90a7ba6", "openfda": {"upc": ["0368071236866"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["bdade691-3687-3308-e053-2995a90ad6ed"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-2368-6)", "package_ndc": "68071-2368-6", "marketing_start_date": "20210316"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "68071-2368_4b455e52-2501-d55a-e063-6294a90a7ba6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-2368", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202160", "marketing_category": "ANDA", "marketing_start_date": "20120712", "listing_expiration_date": "20271231"}