oxaprozin

Generic: oxaprozin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaprozin
Generic Name oxaprozin
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

oxaprozin 600 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0393
Product ID 71335-0393_115ad76f-3895-41b7-bc5a-a7a0975aca9d
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 713350393
Hyphenated Format 71335-0393

Supplemental Identifiers

RxCUI
312132
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
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2)
  • 14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5)
  • 6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)
source: ndc

Packages (7)

71335-0393-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1) 71335-0393-2 20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2) 71335-0393-3 14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3) 71335-0393-4 60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4) 71335-0393-5 90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5) 71335-0393-6 6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6) 71335-0393-7 120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)

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": "115ad76f-3895-41b7-bc5a-a7a0975aca9d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["MHJ80W9LRB"], "rxcui": ["312132"], "spl_set_id": ["dcb85e40-3427-4e56-910d-c1b07bb5c0fa"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1)", "package_ndc": "71335-0393-1", "marketing_start_date": "20070912"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2)", "package_ndc": "71335-0393-2", "marketing_start_date": "20070912"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3)", "package_ndc": "71335-0393-3", "marketing_start_date": "20070912"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4)", "package_ndc": "71335-0393-4", "marketing_start_date": "20070912"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5)", "package_ndc": "71335-0393-5", "marketing_start_date": "20070912"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6)", "package_ndc": "71335-0393-6", "marketing_start_date": "20070912"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)", "package_ndc": "71335-0393-7", "marketing_start_date": "20070912"}], "brand_name": "Oxaprozin", "product_id": "71335-0393_115ad76f-3895-41b7-bc5a-a7a0975aca9d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-0393", "generic_name": "Oxaprozin", "labeler_name": "Bryant Ranch Prepack", "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"}