topiramate

Generic: topiramate

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

Drug Facts

Product Profile

Brand Name topiramate
Generic Name topiramate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

topiramate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7468
Product ID 68788-7468_0174a6bd-1a4a-44b0-a9d3-d45c6ad9514d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078235
Listing Expiration 2026-12-31
Marketing Start 2020-03-02

Pharmacologic Class

Mechanism of Action
cytochrome p450 3a4 inducers [moa] cytochrome p450 2c19 inhibitors [moa]
Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887468
Hyphenated Format 68788-7468

Supplemental Identifiers

RxCUI
199889
UNII
0H73WJJ391
NUI
N0000008486 N0000185506 N0000182140

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 topiramate (source: ndc)
Generic Name topiramate (source: ndc)
Application Number ANDA078235 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7468-3)
  • 15 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)
source: ndc

Packages (4)

68788-7468-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7468-3) 68788-7468-5 15 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5) 68788-7468-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6) 68788-7468-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)

Ingredients (1)

topiramate (100 mg/1)

Linked Drug Pages (1)

topiramate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0174a6bd-1a4a-44b0-a9d3-d45c6ad9514d", "openfda": {"nui": ["N0000008486", "N0000185506", "N0000182140"], "unii": ["0H73WJJ391"], "rxcui": ["199889"], "spl_set_id": ["be42ed09-350c-4e8a-aff4-6afb242dd599"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_moa": ["Cytochrome P450 3A4 Inducers [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7468-3)", "package_ndc": "68788-7468-3", "marketing_start_date": "20200302"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5)", "package_ndc": "68788-7468-5", "marketing_start_date": "20200302"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6)", "package_ndc": "68788-7468-6", "marketing_start_date": "20200302"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)", "package_ndc": "68788-7468-9", "marketing_start_date": "20200302"}], "brand_name": "topiramate", "product_id": "68788-7468_0174a6bd-1a4a-44b0-a9d3-d45c6ad9514d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68788-7468", "generic_name": "topiramate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "topiramate", "active_ingredients": [{"name": "TOPIRAMATE", "strength": "100 mg/1"}], "application_number": "ANDA078235", "marketing_category": "ANDA", "marketing_start_date": "20200302", "listing_expiration_date": "20261231"}