Package 0071-0237-24

Brand: zarontin

Generic: ethosuximide
NDC Package

Package Facts

Identity

Package NDC 0071-0237-24
Digits Only 0071023724
Product NDC 0071-0237
Description

100 CAPSULE in 1 BOTTLE (0071-0237-24)

Marketing

Marketing Status
Marketed Since 2000-09-22
Brand zarontin
Generic ethosuximide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b98eee67-87bf-4ee3-b210-9f6190fdeae5", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0300710237247"], "unii": ["5SEH9X1D1D"], "rxcui": ["197682", "201737"], "spl_set_id": ["0e008f33-70a1-4bc6-b3a0-d45214418ab6"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Parke-Davis Div of Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0071-0237-24)", "package_ndc": "0071-0237-24", "marketing_start_date": "20000922"}], "brand_name": "Zarontin", "product_id": "0071-0237_b98eee67-87bf-4ee3-b210-9f6190fdeae5", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0071-0237", "generic_name": "Ethosuximide", "labeler_name": "Parke-Davis Div of Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zarontin", "active_ingredients": [{"name": "ETHOSUXIMIDE", "strength": "250 mg/1"}], "application_number": "NDA012380", "marketing_category": "NDA", "marketing_start_date": "20000922", "listing_expiration_date": "20261231"}