treximet

Generic: sumatriptan succinate and naproxen sodium

Labeler: currax pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name treximet
Generic Name sumatriptan succinate and naproxen sodium
Labeler currax pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 500 mg/1, sumatriptan succinate 85 mg/1

Manufacturer
Currax Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 42847-850
Product ID 42847-850_ed866a98-f50a-48af-8ad7-9b139a8a6bc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021926
Listing Expiration 2026-12-31
Marketing Start 2008-04-25

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc] serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42847850
Hyphenated Format 42847-850

Supplemental Identifiers

RxCUI
849450 849452
UPC
0342847850098
UNII
9TN87S3A3C J8BDZ68989

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 treximet (source: ndc)
Generic Name sumatriptan succinate and naproxen sodium (source: ndc)
Application Number NDA021926 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 85 mg/1
source: ndc
Packaging
  • 9 TABLET, FILM COATED in 1 BOTTLE (42847-850-09)
source: ndc

Packages (1)

42847-850-09 9 TABLET, FILM COATED in 1 BOTTLE (42847-850-09)

Ingredients (2)

naproxen sodium (500 mg/1) sumatriptan succinate (85 mg/1)

Linked Drug Pages (1)

Treximet ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ed866a98-f50a-48af-8ad7-9b139a8a6bc5", "openfda": {"upc": ["0342847850098"], "unii": ["9TN87S3A3C", "J8BDZ68989"], "rxcui": ["849450", "849452"], "spl_set_id": ["42ddf376-8dc0-4236-be2a-0c6ae92ece04"], "manufacturer_name": ["Currax Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (42847-850-09)", "package_ndc": "42847-850-09", "marketing_start_date": "20080425"}], "brand_name": "Treximet", "product_id": "42847-850_ed866a98-f50a-48af-8ad7-9b139a8a6bc5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "42847-850", "generic_name": "Sumatriptan Succinate and Naproxen Sodium", "labeler_name": "Currax Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Treximet", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "500 mg/1"}, {"name": "SUMATRIPTAN SUCCINATE", "strength": "85 mg/1"}], "application_number": "NDA021926", "marketing_category": "NDA", "marketing_start_date": "20080425", "listing_expiration_date": "20261231"}