felbamate

Generic: felbamate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name felbamate
Generic Name felbamate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

felbamate 600 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1771
Product ID 72162-1771_10aad5f2-8c25-41db-a114-9cbbe9819899
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202284
Listing Expiration 2026-12-31
Marketing Start 2018-09-04

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 721621771
Hyphenated Format 72162-1771

Supplemental Identifiers

RxCUI
198359
UNII
X72RBB02N8
NUI
N0000175753 N0000008486

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 felbamate (source: ndc)
Generic Name felbamate (source: ndc)
Application Number ANDA202284 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-1771-1)
source: ndc

Packages (1)

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

Ingredients (1)

felbamate (600 mg/1)

Linked Drug Pages (1)

Felbamate ndc-match (0.9)

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"}