oxycodone and acetaminophen (31722-192)

Drug Facts

Product Profile

Brand Name oxycodone and acetaminophen

Generic Name oxycodone and acetaminophen

Labeler camber pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

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

Manufacturer

Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-192

Product ID 31722-192_560e8cac-91f2-47dc-ac17-4d511598c49a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207419

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2017-04-11

Pharmacologic Class

Classes

full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722192

Hyphenated Format 31722-192

Supplemental Identifiers

RxCUI

1049214 1049221 1049225 1049635

UPC

0331722194013 0331722191012 0331722192019

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 oxycodone and acetaminophen (source: ndc)

Generic Name oxycodone and acetaminophen (source: ndc)

Application Number ANDA207419 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

325 mg/1
5 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (31722-192-01)
500 TABLET in 1 BOTTLE (31722-192-05)

source: ndc

Packages (2)

31722-192-01 100 TABLET in 1 BOTTLE (31722-192-01) 31722-192-05 500 TABLET in 1 BOTTLE (31722-192-05)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (5 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": "560e8cac-91f2-47dc-ac17-4d511598c49a", "openfda": {"upc": ["0331722194013", "0331722191012", "0331722192019"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["2a49ee34-6f1d-4ed3-8daa-343723d2a2be"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-192-01)", "package_ndc": "31722-192-01", "marketing_start_date": "20170411"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-192-05)", "package_ndc": "31722-192-05", "marketing_start_date": "20170411"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "31722-192_560e8cac-91f2-47dc-ac17-4d511598c49a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-192", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}