Package 69452-152-20

Brand: ethosuximide

Generic: ethosuximide
NDC Package

Package Facts

Identity

Package NDC 69452-152-20
Digits Only 6945215220
Product NDC 69452-152
Product ID 69452-152_0d82d9c4-814d-ed9b-e063-6294a90a6522
Description

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

Marketing

Marketing Status
Marketed Since 2016-10-21
Brand ethosuximide
Generic ethosuximide
Sample Package No

Linked Drug Pages (1)

Ethosuximide ndc-match (0.95)

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"}