felbamate
Generic: felbamate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
felbamate
Generic Name
felbamate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
felbamate 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-1937
Product ID
63629-1937_0f63e531-be6e-4586-8b30-4968dbccf9cb
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636291937
Hyphenated Format
63629-1937
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (63629-1937-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0f63e531-be6e-4586-8b30-4968dbccf9cb", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["X72RBB02N8"], "rxcui": ["198358"], "spl_set_id": ["6afd77f2-4525-42f4-a4b1-94159c401dd2"], "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 (63629-1937-1)", "package_ndc": "63629-1937-1", "marketing_start_date": "20210114"}], "brand_name": "Felbamate", "product_id": "63629-1937_0f63e531-be6e-4586-8b30-4968dbccf9cb", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-1937", "generic_name": "Felbamate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felbamate", "active_ingredients": [{"name": "FELBAMATE", "strength": "400 mg/1"}], "application_number": "ANDA202284", "marketing_category": "ANDA", "marketing_start_date": "20180904", "listing_expiration_date": "20261231"}