oxcarbazepine

Generic: oxcarbazepine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxcarbazepine
Generic Name oxcarbazepine
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

oxcarbazepine 150 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-411
Product ID 71205-411_0f92415d-6d81-4cc1-9a3b-028430951eb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077802
Listing Expiration 2026-12-31
Marketing Start 2007-10-09

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 71205411
Hyphenated Format 71205-411

Supplemental Identifiers

RxCUI
312136
UNII
VZI5B1W380
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 oxcarbazepine (source: ndc)
Generic Name oxcarbazepine (source: ndc)
Application Number ANDA077802 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-411-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-411-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)
source: ndc

Packages (3)

71205-411-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-411-30) 71205-411-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-411-60) 71205-411-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)

Ingredients (1)

oxcarbazepine (150 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": "0f92415d-6d81-4cc1-9a3b-028430951eb8", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["95867dcd-fd0e-4570-987b-d35939f7d7d1"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-411-30)", "package_ndc": "71205-411-30", "marketing_start_date": "20200226"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-411-60)", "package_ndc": "71205-411-60", "marketing_start_date": "20200226"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)", "package_ndc": "71205-411-90", "marketing_start_date": "20200226"}], "brand_name": "Oxcarbazepine", "product_id": "71205-411_0f92415d-6d81-4cc1-9a3b-028430951eb8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-411", "generic_name": "Oxcarbazepine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA077802", "marketing_category": "ANDA", "marketing_start_date": "20071009", "listing_expiration_date": "20261231"}