oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/5mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-406
Product ID 60687-406_30ca5ab4-1e96-888b-e063-6294a90abae0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204037
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2019-04-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687406
Hyphenated Format 60687-406

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 ANDA204037 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 5 TRAY in 1 CASE (60687-406-67) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)
  • 4 TRAY in 1 CASE (60687-406-77) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)
source: ndc

Packages (2)

60687-406-67 5 TRAY in 1 CASE (60687-406-67) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40) 60687-406-77 4 TRAY in 1 CASE (60687-406-77) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)

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": "30ca5ab4-1e96-888b-e063-6294a90abae0", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049604"], "spl_set_id": ["0a6b0659-6816-4f44-81bd-9bac4da5380d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (60687-406-67)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)", "package_ndc": "60687-406-67", "marketing_start_date": "20190422"}, {"sample": false, "description": "4 TRAY in 1 CASE (60687-406-77)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)", "package_ndc": "60687-406-77", "marketing_start_date": "20190422"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "60687-406_30ca5ab4-1e96-888b-e063-6294a90abae0", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-406", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA204037", "marketing_category": "ANDA", "marketing_start_date": "20190422", "listing_expiration_date": "20261231"}