ethosuximide

Generic: ethosuximide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethosuximide
Generic Name ethosuximide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ethosuximide 250 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-532
Product ID 23155-532_b7244494-bae5-4434-9b8f-d5ed6d33619a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200892
Listing Expiration 2026-12-31
Marketing Start 2015-09-09

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 23155532
Hyphenated Format 23155-532

Supplemental Identifiers

RxCUI
197682
UPC
0323155532012
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 ANDA200892 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (23155-532-01)
  • 500 CAPSULE in 1 BOTTLE (23155-532-05)
source: ndc

Packages (2)

23155-532-01 100 CAPSULE in 1 BOTTLE (23155-532-01) 23155-532-05 500 CAPSULE in 1 BOTTLE (23155-532-05)

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": "b7244494-bae5-4434-9b8f-d5ed6d33619a", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0323155532012"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682"], "spl_set_id": ["0d0965f7-d780-4d1c-8ecf-77387483cc02"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (23155-532-01)", "package_ndc": "23155-532-01", "marketing_start_date": "20150909"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (23155-532-05)", "package_ndc": "23155-532-05", "marketing_start_date": "20150909"}], "brand_name": "ETHOSUXIMIDE", "product_id": "23155-532_b7244494-bae5-4434-9b8f-d5ed6d33619a", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "23155-532", "generic_name": "ETHOSUXIMIDE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETHOSUXIMIDE", "active_ingredients": [{"name": "ETHOSUXIMIDE", "strength": "250 mg/1"}], "application_number": "ANDA200892", "marketing_category": "ANDA", "marketing_start_date": "20150909", "listing_expiration_date": "20261231"}