Package 42806-708-01
Brand: ethosuximide
Generic: ethosuximidePackage Facts
Identity
Package NDC
42806-708-01
Digits Only
4280670801
Product NDC
42806-708
Description
100 CAPSULE in 1 BOTTLE (42806-708-01)
Marketing
Marketing Status
Brand
ethosuximide
Generic
ethosuximide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b206d5a-4881-923b-e063-6294a90a13b5", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682"], "spl_set_id": ["85c50760-98cc-4888-b27f-146937acc893"], "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 (42806-708-01)", "package_ndc": "42806-708-01", "marketing_start_date": "20211112"}], "brand_name": "Ethosuximide", "product_id": "42806-708_2b206d5a-4881-923b-e063-6294a90a13b5", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "42806-708", "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": "20211112", "listing_expiration_date": "20261231"}