ethosuximide

Generic: ethosuximide

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethosuximide
Generic Name ethosuximide
Labeler epic pharma, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ethosuximide 250 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-711
Product ID 42806-711_2b366128-2db7-bb4e-e063-6294a90af2d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210654
Listing Expiration 2026-12-31
Marketing Start 2020-03-16

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 42806711
Hyphenated Format 42806-711

Supplemental Identifiers

RxCUI
197682
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 ANDA210654 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (42806-711-01)
source: ndc

Packages (1)

42806-711-01 100 CAPSULE in 1 BOTTLE (42806-711-01)

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": "2b366128-2db7-bb4e-e063-6294a90af2d7", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682"], "spl_set_id": ["a040dab2-0d70-4c02-a830-5ba1e3506a1b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42806-711-01)", "package_ndc": "42806-711-01", "marketing_start_date": "20200415"}], "brand_name": "Ethosuximide", "product_id": "42806-711_2b366128-2db7-bb4e-e063-6294a90af2d7", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "42806-711", "generic_name": "Ethosuximide", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethosuximide", "active_ingredients": [{"name": "ETHOSUXIMIDE", "strength": "250 mg/1"}], "application_number": "ANDA210654", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20261231"}