ethosuximide

Generic: ethosuximide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethosuximide
Generic Name ethosuximide
Labeler bryant ranch prepack
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

ethosuximide 250 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8005
Product ID 63629-8005_e5905131-91d2-403b-948c-da995b7ebebc
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 636298005
Hyphenated Format 63629-8005

Supplemental Identifiers

RxCUI
197682
UNII
5SEH9X1D1D
NUI
N0000175753 N0000008486

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
  • 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-8005-1)
source: ndc

Packages (1)

63629-8005-1 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-8005-1)

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": "e5905131-91d2-403b-948c-da995b7ebebc", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682"], "spl_set_id": ["867b54c4-4ce4-4c00-a03b-f108f1000e29"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-8005-1)", "package_ndc": "63629-8005-1", "marketing_start_date": "20190509"}], "brand_name": "Ethosuximide", "product_id": "63629-8005_e5905131-91d2-403b-948c-da995b7ebebc", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-8005", "generic_name": "Ethosuximide", "labeler_name": "Bryant Ranch Prepack", "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"}