rufinamide

Generic: rufinamide

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rufinamide
Generic Name rufinamide
Labeler camber pharmaceuticals, inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

rufinamide 40 mg/mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-688
Product ID 31722-688_0d914e03-3610-c662-e063-6294a90a5430
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216841
Listing Expiration 2026-12-31
Marketing Start 2023-12-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722688
Hyphenated Format 31722-688

Supplemental Identifiers

RxCUI
1092357
UNII
WFW942PR79

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 rufinamide (source: ndc)
Generic Name rufinamide (source: ndc)
Application Number ANDA216841 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (31722-688-46) / 460 mL in 1 BOTTLE
source: ndc

Packages (1)

31722-688-46 1 BOTTLE in 1 CARTON (31722-688-46) / 460 mL in 1 BOTTLE

Ingredients (1)

rufinamide (40 mg/mL)

Linked Drug Pages (1)

Rufinamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d914e03-3610-c662-e063-6294a90a5430", "openfda": {"unii": ["WFW942PR79"], "rxcui": ["1092357"], "spl_set_id": ["1c2f9bf2-1711-4975-af02-32614db25add"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-688-46)  / 460 mL in 1 BOTTLE", "package_ndc": "31722-688-46", "marketing_start_date": "20231205"}], "brand_name": "Rufinamide", "product_id": "31722-688_0d914e03-3610-c662-e063-6294a90a5430", "dosage_form": "SUSPENSION", "product_ndc": "31722-688", "generic_name": "Rufinamide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rufinamide", "active_ingredients": [{"name": "RUFINAMIDE", "strength": "40 mg/mL"}], "application_number": "ANDA216841", "marketing_category": "ANDA", "marketing_start_date": "20231205", "listing_expiration_date": "20261231"}