oxcarbazepine

Generic: oxcarbazepine

Labeler: xlcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxcarbazepine
Generic Name oxcarbazepine
Labeler xlcare pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

oxcarbazepine 600 mg/1

Manufacturer
XLCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72865-285
Product ID 72865-285_1d5c79a3-4eec-f65b-e063-6294a90aab4f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215939
Listing Expiration 2026-12-31
Marketing Start 2024-07-18

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 72865285
Hyphenated Format 72865-285

Supplemental Identifiers

RxCUI
312136 312137 312138
UPC
0372865284018 0372865285015 0372865283011
UNII
VZI5B1W380
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 oxcarbazepine (source: ndc)
Generic Name oxcarbazepine (source: ndc)
Application Number ANDA215939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (72865-285-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (72865-285-05)
source: ndc

Packages (2)

72865-285-01 100 TABLET, FILM COATED in 1 BOTTLE (72865-285-01) 72865-285-05 500 TABLET, FILM COATED in 1 BOTTLE (72865-285-05)

Ingredients (1)

oxcarbazepine (600 mg/1)

Linked Drug Pages (1)

Oxcarbazepine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d5c79a3-4eec-f65b-e063-6294a90aab4f", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0372865284018", "0372865285015", "0372865283011"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["9f5d17e4-ca68-48e2-9e87-d3ab1c59aa93"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72865-285-01)", "package_ndc": "72865-285-01", "marketing_start_date": "20240718"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72865-285-05)", "package_ndc": "72865-285-05", "marketing_start_date": "20240718"}], "brand_name": "Oxcarbazepine", "product_id": "72865-285_1d5c79a3-4eec-f65b-e063-6294a90aab4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72865-285", "generic_name": "Oxcarbazepine", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "600 mg/1"}], "application_number": "ANDA215939", "marketing_category": "ANDA", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}