felbamate

Generic: felbamate

Labeler: taro pharmaceuticals u.s.a., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name felbamate
Generic Name felbamate
Labeler taro pharmaceuticals u.s.a., inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

felbamate 600 mg/1

Manufacturer
Taro Pharmaceuticals U.S.A., inc.

Identifiers & Regulatory

Product NDC 51672-4186
Product ID 51672-4186_0c6d8e37-6982-22d4-e063-6294a90a4f6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207093
Listing Expiration 2026-12-31
Marketing Start 2017-04-20

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 516724186
Hyphenated Format 51672-4186

Supplemental Identifiers

RxCUI
198358 198359
UNII
X72RBB02N8
NUI
N0000175753 N0000008486

Packaging Origin

Original Packager
true

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 ANDA207093 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (51672-4186-1)
  • 90 TABLET in 1 BOTTLE (51672-4186-5)
  • 30 TABLET in 1 BOTTLE (51672-4186-6)
source: ndc

Packages (3)

51672-4186-1 100 TABLET in 1 BOTTLE (51672-4186-1) 51672-4186-5 90 TABLET in 1 BOTTLE (51672-4186-5) 51672-4186-6 30 TABLET in 1 BOTTLE (51672-4186-6)

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": "0c6d8e37-6982-22d4-e063-6294a90a4f6b", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["X72RBB02N8"], "rxcui": ["198358", "198359"], "spl_set_id": ["f2edb3ed-da20-4093-88ea-00fe781e47e0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4186-1)", "package_ndc": "51672-4186-1", "marketing_start_date": "20170420"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (51672-4186-5)", "package_ndc": "51672-4186-5", "marketing_start_date": "20231215"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51672-4186-6)", "package_ndc": "51672-4186-6", "marketing_start_date": "20170420"}], "brand_name": "Felbamate", "product_id": "51672-4186_0c6d8e37-6982-22d4-e063-6294a90a4f6b", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51672-4186", "generic_name": "Felbamate", "labeler_name": "Taro Pharmaceuticals U.S.A., inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felbamate", "active_ingredients": [{"name": "FELBAMATE", "strength": "600 mg/1"}], "application_number": "ANDA207093", "marketing_category": "ANDA", "marketing_start_date": "20170420", "listing_expiration_date": "20261231"}