endocet

Generic: oxycodone and acetaminophen

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name endocet
Generic Name oxycodone and acetaminophen
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, oxycodone hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1728
Product ID 72162-1728_3b346ded-0a03-4fea-933c-5b3e1ccd2a70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040330
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2003-03-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621728
Hyphenated Format 72162-1728

Supplemental Identifiers

RxCUI
1049214 1049216
UNII
362O9ITL9D 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 endocet (source: ndc)
Generic Name oxycodone and acetaminophen (source: ndc)
Application Number ANDA040330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-1728-1)
source: ndc

Packages (1)

72162-1728-1 100 TABLET in 1 BOTTLE (72162-1728-1)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

ENDOCET ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b346ded-0a03-4fea-933c-5b3e1ccd2a70", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214", "1049216"], "spl_set_id": ["7dc10b86-c6cd-4012-b7b9-b694ccf4f768"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1728-1)", "package_ndc": "72162-1728-1", "marketing_start_date": "20240827"}], "brand_name": "ENDOCET", "product_id": "72162-1728_3b346ded-0a03-4fea-933c-5b3e1ccd2a70", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1728", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENDOCET", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "20030306", "listing_expiration_date": "20261231"}