nalocet

Generic: oxycodone and acetaminophen

Labeler: forte bio-pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nalocet
Generic Name oxycodone and acetaminophen
Labeler forte bio-pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 300 mg/1, oxycodone hydrochloride 2.5 mg/1

Manufacturer
Forte Bio-Pharma LLC

Identifiers & Regulatory

Product NDC 72245-193
Product ID 72245-193_1f08bded-8a63-5cb4-e063-6294a90a0a7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040608
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2018-05-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72245193
Hyphenated Format 72245-193

Supplemental Identifiers

RxCUI
1037259 2045500
UNII
362O9ITL9D C1ENJ2TE6C

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 nalocet (source: ndc)
Generic Name oxycodone and acetaminophen (source: ndc)
Application Number ANDA040608 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03)
  • 100 TABLET in 1 BOTTLE, PLASTIC (72245-193-10)
source: ndc

Packages (2)

Ingredients (2)

acetaminophen (300 mg/1) oxycodone hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f08bded-8a63-5cb4-e063-6294a90a0a7a", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1037259", "2045500"], "spl_set_id": ["f5f7dfca-a5c7-4445-8a5e-9ec62f33f5be"], "manufacturer_name": ["Forte Bio-Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03)", "package_ndc": "72245-193-03", "marketing_start_date": "20180523"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72245-193-10)", "package_ndc": "72245-193-10", "marketing_start_date": "20180523"}], "brand_name": "Nalocet", "product_id": "72245-193_1f08bded-8a63-5cb4-e063-6294a90a0a7a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72245-193", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Forte Bio-Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalocet", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA040608", "marketing_category": "ANDA", "marketing_start_date": "20180523", "listing_expiration_date": "20261231"}