oxaprozin

Generic: oxaprozin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaprozin
Generic Name oxaprozin
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

oxaprozin 600 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-261
Product ID 82804-261_e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075855
Listing Expiration 2026-12-31
Marketing Start 2001-01-31

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804261
Hyphenated Format 82804-261

Supplemental Identifiers

RxCUI
312132
UPC
0382804261604
UNII
MHJ80W9LRB
NUI
N0000000160 M0001335 N0000175722

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 oxaprozin (source: ndc)
Generic Name oxaprozin (source: ndc)
Application Number ANDA075855 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (82804-261-60)
source: ndc

Packages (1)

82804-261-60 60 TABLET, FILM COATED in 1 BOTTLE (82804-261-60)

Ingredients (1)

oxaprozin (600 mg/1)

Linked Drug Pages (1)

Oxaprozin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0382804261604"], "unii": ["MHJ80W9LRB"], "rxcui": ["312132"], "spl_set_id": ["e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-261-60)", "package_ndc": "82804-261-60", "marketing_start_date": "20251212"}], "brand_name": "Oxaprozin", "product_id": "82804-261_e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82804-261", "generic_name": "Oxaprozin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaprozin", "active_ingredients": [{"name": "OXAPROZIN", "strength": "600 mg/1"}], "application_number": "ANDA075855", "marketing_category": "ANDA", "marketing_start_date": "20010131", "listing_expiration_date": "20261231"}