oxycodone and acetaminophen
Generic: oxycodone and acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
oxycodone and acetaminophen
Generic Name
oxycodone and acetaminophen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1, oxycodone hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-8879
Product ID
63629-8879_f15258bd-bf40-4307-8af1-ad8f84440f6d
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636298879
Hyphenated Format
63629-8879
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (63629-8879-1)
- 90 TABLET in 1 BOTTLE, PLASTIC (63629-8879-2)
- 60 TABLET in 1 BOTTLE, PLASTIC (63629-8879-3)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f15258bd-bf40-4307-8af1-ad8f84440f6d", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["626b7834-edb8-4d13-af5c-fff97d4eb9de"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63629-8879-1)", "package_ndc": "63629-8879-1", "marketing_start_date": "20211004"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (63629-8879-2)", "package_ndc": "63629-8879-2", "marketing_start_date": "20211004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (63629-8879-3)", "package_ndc": "63629-8879-3", "marketing_start_date": "20211004"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "63629-8879_f15258bd-bf40-4307-8af1-ad8f84440f6d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8879", "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"}