sumatriptan succinate and naproxen sodium

Generic: sumatriptan succinate and naproxen sodium

Labeler: currax pharmaceuticals llc dba cypress, hawthorn, macoven
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan succinate and naproxen sodium
Generic Name sumatriptan succinate and naproxen sodium
Labeler currax pharmaceuticals llc dba cypress, hawthorn, macoven
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven

Identifiers & Regulatory

Product NDC 44183-850
Product ID 44183-850_e0a82608-7b67-4d15-a04a-16e6c341c621
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021926
Listing Expiration 2026-12-31
Marketing Start 2015-05-14

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 44183850
Hyphenated Format 44183-850

Supplemental Identifiers

RxCUI
849450
UPC
0344183850091
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 sumatriptan succinate and naproxen sodium (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 in 1 BOTTLE (44183-850-09)
source: ndc

Packages (1)

44183-850-09 9 TABLET in 1 BOTTLE (44183-850-09)

Ingredients (2)

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

Linked Drug Pages (1)

Sumatriptan Succinate and Naproxen Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e0a82608-7b67-4d15-a04a-16e6c341c621", "openfda": {"upc": ["0344183850091"], "unii": ["9TN87S3A3C", "J8BDZ68989"], "rxcui": ["849450"], "spl_set_id": ["5762bbe6-bddf-495c-adf8-9096f98a3a9c"], "manufacturer_name": ["Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (44183-850-09)", "package_ndc": "44183-850-09", "marketing_start_date": "20180215"}], "brand_name": "Sumatriptan Succinate and Naproxen Sodium", "product_id": "44183-850_e0a82608-7b67-4d15-a04a-16e6c341c621", "dosage_form": "TABLET", "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": "44183-850", "generic_name": "sumatriptan succinate and naproxen sodium", "labeler_name": "Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate and Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "500 mg/1"}, {"name": "SUMATRIPTAN SUCCINATE", "strength": "85 mg/1"}], "application_number": "NDA021926", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20150514", "listing_expiration_date": "20261231"}