percocet

Generic: oxycodone hydrochloride and acetaminophen

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name percocet
Generic Name oxycodone hydrochloride and acetaminophen
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, oxycodone hydrochloride 5 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 63481-623
Product ID 63481-623_3cbe384a-10a6-4a65-b305-4a466ceed0b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040330
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 1999-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63481623
Hyphenated Format 63481-623

Supplemental Identifiers

RxCUI
1049214 1049221 1049225 1049625 1049635 1049637 1049640 1049642
UPC
0363481623701
UNII
C1ENJ2TE6C 362O9ITL9D

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 percocet (source: ndc)
Generic Name oxycodone hydrochloride and acetaminophen (source: ndc)
Application Number ANDA040330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63481-623-70)
source: ndc

Packages (1)

63481-623-70 100 TABLET in 1 BOTTLE (63481-623-70)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (5 mg/1)

Linked Drug Pages (1)

PERCOCET ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cbe384a-10a6-4a65-b305-4a466ceed0b4", "openfda": {"upc": ["0363481623701"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049625", "1049635", "1049637", "1049640", "1049642"], "spl_set_id": ["4dd36cf5-8f73-404a-8b1d-3bd53bd90c25"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63481-623-70)", "package_ndc": "63481-623-70", "marketing_start_date": "19990630"}], "brand_name": "PERCOCET", "product_id": "63481-623_3cbe384a-10a6-4a65-b305-4a466ceed0b4", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63481-623", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride and acetaminophen", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PERCOCET", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "19990630", "listing_expiration_date": "20271231"}