oxycodone and acetaminophen

Generic: oxycodone and acetaminophen

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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 2.5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-948
Product ID 31722-948_77cf0bd6-7b1c-41ec-825b-0ffd86032537
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 31722948
Hyphenated Format 31722-948

Supplemental Identifiers

RxCUI
1049214 1049221 1049225 1049635
UPC
0331722948012 0331722950015 0331722949019 0331722951012 0331722951050 0331722948050 0331722950053 0331722949057
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
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-948-01)
  • 500 TABLET in 1 BOTTLE (31722-948-05)
source: ndc

Packages (2)

31722-948-01 100 TABLET in 1 BOTTLE (31722-948-01) 31722-948-05 500 TABLET in 1 BOTTLE (31722-948-05)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (2.5 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": "77cf0bd6-7b1c-41ec-825b-0ffd86032537", "openfda": {"upc": ["0331722948012", "0331722950015", "0331722949019", "0331722951012", "0331722951050", "0331722948050", "0331722950053", "0331722949057"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["42777191-0454-4ccb-8fc3-8b18b0ee43f7"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-948-01)", "package_ndc": "31722-948-01", "marketing_start_date": "20190315"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-948-05)", "package_ndc": "31722-948-05", "marketing_start_date": "20190315"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "31722-948_77cf0bd6-7b1c-41ec-825b-0ffd86032537", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-948", "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": "2.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}