Package 72162-1771-1

Brand: felbamate

Generic: felbamate
NDC Package

Package Facts

Identity

Package NDC 72162-1771-1
Digits Only 7216217711
Product NDC 72162-1771
Description

100 TABLET in 1 BOTTLE (72162-1771-1)

Marketing

Marketing Status
Marketed Since 2023-08-30
Brand felbamate
Generic felbamate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10aad5f2-8c25-41db-a114-9cbbe9819899", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["X72RBB02N8"], "rxcui": ["198359"], "spl_set_id": ["696e3cbb-a431-4f29-acbd-1db8e9aaef93"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1771-1)", "package_ndc": "72162-1771-1", "marketing_start_date": "20230830"}], "brand_name": "Felbamate", "product_id": "72162-1771_10aad5f2-8c25-41db-a114-9cbbe9819899", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1771", "generic_name": "Felbamate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felbamate", "active_ingredients": [{"name": "FELBAMATE", "strength": "600 mg/1"}], "application_number": "ANDA202284", "marketing_category": "ANDA", "marketing_start_date": "20180904", "listing_expiration_date": "20261231"}