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NDC 62756-0185-83 Oxcarbazepine 600 mg/1 Details

Oxcarbazepine 600 mg/1

Oxcarbazepine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is OXCARBAZEPINE.

MedlinePlus Drug Summary

Oxcarbazepine (Trileptal) is used alone or in combination with other medications to control certain types of seizures in adults and children. Oxcarbazepine extended-release tablets (Oxtellar XR) are used in combination with other medications to control certain types of seizures in adults and children 6 years of age and older. Oxcarbazepine is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.

Related Packages: 62756-0185-83
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Oxcarbazepine

Product Information

NDC	62756-0185
Product ID	62756-185_5cee2e11-dc01-4ea5-aa6b-b07bba5f3400
Associated GPIs	72600046000340
GCN Sequence Number	027780
GCN Sequence Number Description	oxcarbazepine TABLET 600 MG ORAL
HIC3	H4B
HIC3 Description	ANTICONVULSANTS
GCN	21722
HICL Sequence Number	011735
HICL Sequence Number Description	OXCARBAZEPINE
Brand/Generic	Generic
Proprietary Name	Oxcarbazepine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Oxcarbazepine
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	600
Active Ingredient Units	mg/1
Substance Name	OXCARBAZEPINE
Labeler Name	Sun Pharmaceutical Industries, Inc.
Pharmaceutical Class	Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077794
Listing Certified Through	2024-12-31

Package

NDC 62756-0185-83 (62756018583)

Pricing Information	N/A
NDC Package Code	62756-185-83
Billing NDC	62756018583
Package	30 TABLET, FILM COATED in 1 BOTTLE (62756-185-83)
Marketing Start Date	2007-10-09
NDC Exclude Flag	N