oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: camber pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler camber pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 20 mg/1

Manufacturer
Camber Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 31722-486
Product ID 31722-486_a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207418
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2025-11-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722486
Hyphenated Format 31722-486

Supplemental Identifiers

RxCUI
1049611 1049618 1049621 1049683 1049686
UPC
0331722917018 0331722485050 0331722486019 0331722918053 0331722484053 0331722486057 0331722485012 0331722917056 0331722484015 0331722918015
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 ANDA207418 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-486-01)
  • 500 TABLET in 1 BOTTLE (31722-486-05)
source: ndc

Packages (2)

31722-486-01 100 TABLET in 1 BOTTLE (31722-486-01) 31722-486-05 500 TABLET in 1 BOTTLE (31722-486-05)

Ingredients (1)

oxycodone hydrochloride (20 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": "a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e", "openfda": {"upc": ["0331722917018", "0331722485050", "0331722486019", "0331722918053", "0331722484053", "0331722486057", "0331722485012", "0331722917056", "0331722484015", "0331722918015"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["01db4606-d49c-4b10-a78a-1cf41880a9fb"], "manufacturer_name": ["Camber Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-486-01)", "package_ndc": "31722-486-01", "marketing_start_date": "20251114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-486-05)", "package_ndc": "31722-486-05", "marketing_start_date": "20251114"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "31722-486_a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-486", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Camber Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20251114", "listing_expiration_date": "20271231"}