oxycodone and acetaminophen (63629-8876)

Drug Facts

Product Profile

Brand Name oxycodone and acetaminophen

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 63629-8876

Product ID 63629-8876_a09c945c-9621-49a8-9b04-acea348af0cf

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA201278

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2014-08-28

Pharmacologic Class

Classes

full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636298876

Hyphenated Format 63629-8876

Supplemental Identifiers

RxCUI

1049214

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 oxycodone and acetaminophen (source: ndc)

Generic Name oxycodone and acetaminophen (source: ndc)

Application Number ANDA201278 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

325 mg/1
10 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE, PLASTIC (63629-8876-1)

source: ndc

Packages (1)

63629-8876-1 100 TABLET in 1 BOTTLE, PLASTIC (63629-8876-1)

Ingredients (2)

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

Linked Drug Pages (1)

Oxycodone and Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "a09c945c-9621-49a8-9b04-acea348af0cf", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["639aba0b-1ef6-415f-9732-ebf52bcc1b86"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-8876-1)", "package_ndc": "63629-8876-1", "marketing_start_date": "20211001"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "63629-8876_a09c945c-9621-49a8-9b04-acea348af0cf", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8876", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20261231"}