topiramate

Generic: topiramate

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

Drug Facts

Product Profile

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

topiramate 25 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-1971
Product ID 68071-1971_3ab5a044-1530-14af-e063-6394a90a35ca
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076343
Listing Expiration 2026-12-31
Marketing Start 2014-06-12

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 680711971
Hyphenated Format 68071-1971

Supplemental Identifiers

RxCUI
199888
UPC
0368071197198
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 ANDA076343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-1971-3)
  • 60 TABLET in 1 BOTTLE (68071-1971-6)
  • 90 TABLET in 1 BOTTLE (68071-1971-9)
source: ndc

Packages (3)

68071-1971-3 30 TABLET in 1 BOTTLE (68071-1971-3) 68071-1971-6 60 TABLET in 1 BOTTLE (68071-1971-6) 68071-1971-9 90 TABLET in 1 BOTTLE (68071-1971-9)

Ingredients (1)

topiramate (25 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": "3ab5a044-1530-14af-e063-6394a90a35ca", "openfda": {"nui": ["N0000008486", "N0000185506", "N0000182140"], "upc": ["0368071197198"], "unii": ["0H73WJJ391"], "rxcui": ["199888"], "spl_set_id": ["490f109f-30cb-0790-e054-00144ff88e88"], "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": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-1971-3)", "package_ndc": "68071-1971-3", "marketing_start_date": "20170221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-1971-6)", "package_ndc": "68071-1971-6", "marketing_start_date": "20170221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-1971-9)", "package_ndc": "68071-1971-9", "marketing_start_date": "20170221"}], "brand_name": "Topiramate", "product_id": "68071-1971_3ab5a044-1530-14af-e063-6394a90a35ca", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68071-1971", "generic_name": "Topiramate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Topiramate", "active_ingredients": [{"name": "TOPIRAMATE", "strength": "25 mg/1"}], "application_number": "ANDA076343", "marketing_category": "ANDA", "marketing_start_date": "20140612", "listing_expiration_date": "20261231"}