ethosuximide

Generic: ethosuximide

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

Drug Facts

Product Profile

Brand Name ethosuximide
Generic Name ethosuximide
Labeler bionpharma inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

ethosuximide 250 mg/1

Manufacturer
Bionpharma Inc.

Identifiers & Regulatory

Product NDC 69452-152
Product ID 69452-152_0d82d9c4-814d-ed9b-e063-6294a90a6522
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040430
Listing Expiration 2026-12-31
Marketing Start 2016-10-21

Pharmacologic Class

Established (EPC)
anti-epileptic agent [epc]
Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69452152
Hyphenated Format 69452-152

Supplemental Identifiers

RxCUI
197682
UPC
0369452152201
UNII
5SEH9X1D1D
NUI
N0000175753 N0000008486

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 ethosuximide (source: ndc)
Generic Name ethosuximide (source: ndc)
Application Number ANDA040430 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-152-20)
source: ndc

Packages (1)

69452-152-20 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-152-20)

Ingredients (1)

ethosuximide (250 mg/1)

Linked Drug Pages (1)

Ethosuximide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d82d9c4-814d-ed9b-e063-6294a90a6522", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0369452152201"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682"], "spl_set_id": ["efb047e8-0020-4504-97fa-6aa1af3af05e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-152-20)", "package_ndc": "69452-152-20", "marketing_start_date": "20161021"}], "brand_name": "Ethosuximide", "product_id": "69452-152_0d82d9c4-814d-ed9b-e063-6294a90a6522", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "69452-152", "generic_name": "Ethosuximide", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethosuximide", "active_ingredients": [{"name": "ETHOSUXIMIDE", "strength": "250 mg/1"}], "application_number": "ANDA040430", "marketing_category": "ANDA", "marketing_start_date": "20161021", "listing_expiration_date": "20261231"}